| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001265597.2 | 419 | Missense Mutation | GCA,GTA | A80V | NP_001252526.1 |
| NM_001265598.2 | 419 | Missense Mutation | GCA,GTA | A67V | NP_001252527.1 |
| NM_001265599.2 | 419 | Missense Mutation | GCA,GTA | A6V | NP_001252528.1 |
| NM_001265600.2 | 419 | Missense Mutation | GCA,GTA | A6V | NP_001252529.1 |
| NM_001322306.1 | 419 | Intron | NP_001309235.1 | ||
| NM_006385.4 | 419 | Missense Mutation | GCA,GTA | A80V | NP_006376.2 |
| NM_198855.3 | 419 | Missense Mutation | GCA,GTA | A67V | NP_942152.1 |