| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304467.1 | 689 | Missense Mutation | AAT,GAT | N115D | NP_001291396.1 |
| NM_001304468.1 | 689 | Missense Mutation | AAT,GAT | N115D | NP_001291397.1 |
| NM_212554.3 | 689 | Missense Mutation | AAT,GAT | N193D | NP_997719.2 |