| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287595.1 | 1496 | Missense Mutation | AGT,TGT | S604C | NP_001274524.1 |
| NM_001287596.1 | 1496 | Intron | NP_001274525.1 | ||
| NM_001287597.1 | 1496 | UTR 3 | NP_001274526.1 | ||
| NM_006671.5 | 1496 | Missense Mutation | AGT,TGT | S545C | NP_006662.3 |
| XM_011542002.2 | 1496 | Missense Mutation | AGT,TGT | S322C | XP_011540304.1 |