| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281768.1 | 290 | Intron | NP_001268697.1 | ||
| NM_021116.2 | 290 | Missense Mutation | GCC,GTC | A91V | NP_066939.1 |
| XM_005249584.3 | 290 | Missense Mutation | GCC,GTC | A91V | XP_005249641.1 |
| XM_005249585.2 | 290 | Missense Mutation | GCC,GTC | A91V | XP_005249642.1 |