| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_177538.2 | 857 | Missense Mutation | ATT,GTT | I79V | NP_803882.1 |
| XM_005246698.3 | 857 | Intron | XP_005246755.1 | ||
| XM_005246699.3 | 857 | Intron | XP_005246756.1 | ||
| XM_005246701.3 | 857 | Intron | XP_005246758.1 | ||
| XM_006712644.3 | 857 | Missense Mutation | ATT,GTT | I61V | XP_006712707.1 |
| XM_006712645.3 | 857 | Missense Mutation | ATT,GTT | I79V | XP_006712708.1 |
| XM_017004555.1 | 857 | Intron | XP_016860044.1 |