| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318066.1 | 2499 | Missense Mutation | TCT,TGT | S1016C | NP_001304995.1 |
| NM_014822.3 | 2499 | Missense Mutation | TCT,TGT | S1015C | NP_055637.2 |
| XM_005263379.2 | 2499 | Missense Mutation | TCT,TGT | S1016C | XP_005263436.1 |
| XM_017008875.1 | 2499 | Missense Mutation | TCT,TGT | S571C | XP_016864364.1 |