| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015888.4 | 318 | Missense Mutation | GCT,GTT | A41V | NP_056972.1 |
| XM_006710676.1 | 318 | Missense Mutation | GCT,GTT | A41V | XP_006710739.1 |
| XM_011541562.2 | 318 | UTR 5 | XP_011539864.1 | ||
| XM_011541563.1 | 318 | Missense Mutation | GCT,GTT | A41V | XP_011539865.1 |
| XM_017001424.1 | 318 | Missense Mutation | GCT,GTT | A41V | XP_016856913.1 |