| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021035.2 | 4278 | Missense Mutation | GCT,GTT | A1702V | NP_066363.1 |
| XM_006723836.1 | 4278 | Missense Mutation | GCT,GTT | A1702V | XP_006723899.1 |
| XM_011528924.1 | 4278 | Missense Mutation | GCT,GTT | A1652V | XP_011527226.1 |
| XM_017027971.1 | 4278 | Missense Mutation | GCT,GTT | A984V | XP_016883460.1 |