| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001190992.1 | 1779 | Missense Mutation | ATC,GTC | I412V | NP_001177921.1 |
| NM_004733.3 | 1779 | Missense Mutation | ATC,GTC | I412V | NP_004724.1 |
| XM_011513311.2 | 1779 | Intron | XP_011511613.1 | ||
| XM_017007462.1 | 1779 | Intron | XP_016862951.1 | ||
| XM_017007463.1 | 1779 | Missense Mutation | ATC,GTC | I242V | XP_016862952.1 |
| XM_017007464.1 | 1779 | Missense Mutation | ATC,GTC | I141V | XP_016862953.1 |