| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152334.2 | 1690 | Missense Mutation | ATT,GTT | I729V | NP_689547.2 |
| XM_006720386.3 | 1690 | Silent Mutation | ACA,ACG | T704T | XP_006720449.1 |
| XM_017021912.1 | 1690 | Intron | XP_016877401.1 | ||
| XM_017021913.1 | 1690 | Missense Mutation | ATT,GTT | I486V | XP_016877402.1 |