| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143676.1 | 1191 | Missense Mutation | ATC,GTC | I448V | NP_001137148.1 |
| NM_001143677.1 | 1191 | Missense Mutation | ATC,GTC | I381V | NP_001137149.1 |
| NM_001143678.1 | 1191 | Missense Mutation | ATC,GTC | I367V | NP_001137150.1 |
| NM_001291995.1 | 1191 | Missense Mutation | ATC,GTC | I309V | NP_001278924.1 |
| NM_005627.3 | 1191 | Missense Mutation | ATC,GTC | I353V | NP_005618.2 |
| XM_011536071.1 | 1191 | Missense Mutation | ATC,GTC | I448V | XP_011534373.1 |