| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014464.3 | 267 | Missense Mutation | ATT,GTT | I41V | NP_055279.3 |
| XM_006715062.2 | 267 | Missense Mutation | ATT,GTT | I23V | XP_006715125.1 |
| XM_011514497.2 | 267 | Missense Mutation | ATT,GTT | I41V | XP_011512799.1 |
| XM_017010745.1 | 267 | Missense Mutation | ATT,GTT | I41V | XP_016866234.1 |
| XM_017010746.1 | 267 | Missense Mutation | ATT,GTT | I41V | XP_016866235.1 |
| XM_017010747.1 | 267 | Missense Mutation | ATT,GTT | I41V | XP_016866236.1 |
| XM_017010748.1 | 267 | Intron | XP_016866237.1 |