| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318251.1 | 722 | Missense Mutation | ATT,GTT | I207V | NP_001305180.1 |
| NM_175878.4 | 722 | Missense Mutation | ATT,GTT | I207V | NP_787074.2 |
| XM_017028600.1 | 722 | Missense Mutation | ATT,GTT | I207V | XP_016884089.1 |