| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001008779.1 | 322 | Missense Mutation | TGT,TTT | C39F | NP_001008779.1 |
| NM_001142634.1 | 322 | Missense Mutation | TGT,TTT | C39F | NP_001136106.1 |
| NM_182756.3 | 322 | Missense Mutation | TGT,TTT | C39F | NP_877433.2 |