| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303229.1 | 272 | UTR 5 | NP_001290158.1 | ||
| NM_001303242.1 | 272 | Missense Mutation | TCC,TTC | S15F | NP_001290171.1 |
| NM_001303243.1 | 272 | UTR 5 | NP_001290172.1 | ||
| NM_021222.2 | 272 | Missense Mutation | TCC,TTC | S15F | NP_067045.1 |
| XM_005245393.4 | 272 | Missense Mutation | TCC,TTC | S15F | XP_005245450.1 |
| XM_011509832.2 | 272 | Intron | XP_011508134.1 | ||
| XM_017001955.1 | 272 | Missense Mutation | TCC,TTC | S15F | XP_016857444.1 |
| XM_017001956.1 | 272 | UTR 5 | XP_016857445.1 | ||
| XM_017001957.1 | 272 | UTR 5 | XP_016857446.1 |