| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015370.1 | 467 | Missense Mutation | GCC,GTC | A182V | NP_056185.1 |
| XM_005261491.3 | 467 | Missense Mutation | GCC,GTC | A78V | XP_005261548.1 |
| XM_011530096.2 | 467 | Missense Mutation | GCC,GTC | A141V | XP_011528398.1 |
| XM_017028741.1 | 467 | Missense Mutation | GCC,GTC | A141V | XP_016884230.1 |