| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138330.2 | 1054 | Intron | NP_612203.2 | ||
| XM_017026442.1 | 1054 | Missense Mutation | TGT,TTT | C9F | XP_016881931.1 |
| XM_017026443.1 | 1054 | Missense Mutation | TGT,TTT | C9F | XP_016881932.1 |
| XM_017026444.1 | 1054 | Intron | XP_016881933.1 |