SRX14997828 GSM6065842_r1 SRP372252 PRJNA832094 SRS12747023 GSM6065842 GSM6065842 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997829 GSM6065843_r1 SRP372252 PRJNA832094 SRS12747024 GSM6065843 GSM6065843 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997830 GSM6065844_r1 SRP372252 PRJNA832094 SRS12747025 GSM6065844 GSM6065844 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997831 GSM6065845_r1 SRP372252 PRJNA832094 SRS12747026 GSM6065845 GSM6065845 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997832 GSM6065846_r1 SRP372252 PRJNA832094 SRS12747027 GSM6065846 GSM6065846 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997833 GSM6065847_r1 SRP372252 PRJNA832094 SRS12747028 GSM6065847 GSM6065847 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997834 GSM6065848_r1 SRP372252 PRJNA832094 SRS12747029 GSM6065848 GSM6065848 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997835 GSM6065849_r1 SRP372252 PRJNA832094 SRS12747030 GSM6065849 GSM6065849 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997836 GSM6065850_r1 SRP372252 PRJNA832094 SRS12747031 GSM6065850 GSM6065850 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997837 GSM6065851_r1 SRP372252 PRJNA832094 SRS12747032 GSM6065851 GSM6065851 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997838 GSM6065852_r1 SRP372252 PRJNA832094 SRS12747033 GSM6065852 GSM6065852 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997839 GSM6065853_r1 SRP372252 PRJNA832094 SRS12747034 GSM6065853 GSM6065853 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997840 GSM6065854_r1 SRP372252 PRJNA832094 SRS12747035 GSM6065854 GSM6065854 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997841 GSM6065855_r1 SRP372252 PRJNA832094 SRS12747036 GSM6065855 GSM6065855 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997842 GSM6065856_r1 SRP372252 PRJNA832094 SRS12747037 GSM6065856 GSM6065856 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997843 GSM6065857_r1 SRP372252 PRJNA832094 SRS12747038 GSM6065857 GSM6065857 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997844 GSM6065858_r1 SRP372252 PRJNA832094 SRS12747039 GSM6065858 GSM6065858 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997845 GSM6065859_r1 SRP372252 PRJNA832094 SRS12747040 GSM6065859 GSM6065859 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997846 GSM6065860_r1 SRP372252 PRJNA832094 SRS12747041 GSM6065860 GSM6065860 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997847 GSM6065861_r1 SRP372252 PRJNA832094 SRS12747042 GSM6065861 GSM6065861 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997848 GSM6065862_r1 SRP372252 PRJNA832094 SRS12747043 GSM6065862 GSM6065862 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997849 GSM6065863_r1 SRP372252 PRJNA832094 SRS12747044 GSM6065863 GSM6065863 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997850 GSM6065864_r1 SRP372252 PRJNA832094 SRS12747045 GSM6065864 GSM6065864 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997851 GSM6065865_r1 SRP372252 PRJNA832094 SRS12747046 GSM6065865 GSM6065865 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997852 GSM6065866_r1 SRP372252 PRJNA832094 SRS12747047 GSM6065866 GSM6065866 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997853 GSM6065867_r1 SRP372252 PRJNA832094 SRS12747048 GSM6065867 GSM6065867 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997854 GSM6065868_r1 SRP372252 PRJNA832094 SRS12747049 GSM6065868 GSM6065868 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997855 GSM6065869_r1 SRP372252 PRJNA832094 SRS12747050 GSM6065869 GSM6065869 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997856 GSM6065870_r1 SRP372252 PRJNA832094 SRS12747051 GSM6065870 GSM6065870 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997857 GSM6065871_r1 SRP372252 PRJNA832094 SRS12747052 GSM6065871 GSM6065871 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997858 GSM6065872_r1 SRP372252 PRJNA832094 SRS12747053 GSM6065872 GSM6065872 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997859 GSM6065873_r1 SRP372252 PRJNA832094 SRS12747054 GSM6065873 GSM6065873 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997860 GSM6065874_r1 SRP372252 PRJNA832094 SRS12747055 GSM6065874 GSM6065874 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 SRX14997861 GSM6065875_r1 SRP372252 PRJNA832094 SRS12747056 GSM6065875 GSM6065875 RNA-Seq TRANSCRIPTOMIC cDNA Collected tissues were stored at -80°C. RNA was isolated using Trizol reagent. QuantSeq 3′mRNA-Seq Library Prep Kit FWD for Illumina (Lexogen, Vienna, Austria) with 100ng/ul total RNA was used to construct sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550