| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282237.1 | 2594 | Missense Mutation | GCC,GTC | A770V | NP_001269166.1 |
| NM_001282238.1 | 2594 | Missense Mutation | GCC,GTC | A699V | NP_001269167.1 |
| NM_022898.2 | 2594 | Missense Mutation | GCC,GTC | A700V | NP_075049.1 |
| NM_138576.3 | 2594 | Missense Mutation | GCC,GTC | A771V | NP_612808.1 |