| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001306193.1 | 1569 | Missense Mutation | AAT,GAT | N462D | NP_001293122.1 |
| NM_194277.2 | 1569 | Missense Mutation | AAT,GAT | N477D | NP_919253.1 |
| XM_017029947.1 | 1569 | Missense Mutation | AAT,GAT | N461D | XP_016885436.1 |
| XM_017029948.1 | 1569 | Missense Mutation | AAT,GAT | N392D | XP_016885437.1 |
| XM_017029949.1 | 1569 | Missense Mutation | AAT,GAT | N319D | XP_016885438.1 |