| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006451.4 | 1677 | Missense Mutation | CAA,CGA | Q477R | NP_006442.2 |
| NM_182789.3 | 1677 | Missense Mutation | CAA,CGA | Q398R | NP_877590.1 |
| NM_183323.2 | 1677 | Intron | NP_899152.1 | ||
| XM_005248230.3 | 1677 | Intron | XP_005248287.1 | ||
| XM_017008956.1 | 1677 | Intron | XP_016864445.1 |