| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303422.1 | 1554 | Missense Mutation | ATT,GTT | I439V | NP_001290351.1 |
| NM_004490.2 | 1554 | Missense Mutation | ATT,GTT | I526V | NP_004481.2 |
| XM_011511022.2 | 1554 | Intron | XP_011509324.1 | ||
| XM_017003899.1 | 1554 | Missense Mutation | ATT,GTT | I326V | XP_016859388.1 |