| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178505.7 | 1303 | Missense Mutation | CGT,TGT | R312C | NP_848600.2 |
| XM_011539450.2 | 1303 | Intron | XP_011537752.1 | ||
| XM_011539451.1 | 1303 | Intron | XP_011537753.1 | ||
| XM_017015829.1 | 1303 | Intron | XP_016871318.1 |