| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153698.1 | 670 | Missense Mutation | ATT,GTT | I212V | NP_714542.1 |
| XM_005251783.3 | 670 | Missense Mutation | ATT,GTT | I168V | XP_005251840.1 |
| XM_005251784.4 | 670 | Intron | XP_005251841.1 |