| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142393.1 | 2286 | Missense Mutation | GTG,TTG | V707L | NP_001135865.1 |
| NM_001271033.1 | 2286 | Missense Mutation | GTG,TTG | V558L | NP_001257962.1 |
| NM_006403.3 | 2286 | Missense Mutation | GTG,TTG | V707L | NP_006394.1 |
| NM_182966.3 | 2286 | Intron | NP_892011.2 |