| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001128595.2 | 1641 | Missense Mutation | CCA,GCA | P477A | NP_001122067.1 |
| NM_001128596.2 | 1641 | Missense Mutation | CCA,GCA | P477A | NP_001122068.1 |
| NM_001289134.1 | 1641 | Missense Mutation | CCA,GCA | P413A | NP_001276063.1 |
| NM_152332.5 | 1641 | Missense Mutation | CCA,GCA | P477A | NP_689545.1 |