| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_206922.2 | 199 | Missense Mutation | GTG,TTG | V67L | NP_996805.2 |
| XM_005249103.3 | 199 | Missense Mutation | GTG,TTG | V67L | XP_005249160.1 |
| XM_011514609.2 | 199 | Missense Mutation | GTG,TTG | V67L | XP_011512911.1 |
| XM_017010856.1 | 199 | Intron | XP_016866345.1 | ||
| XM_017010857.1 | 199 | Intron | XP_016866346.1 |