| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001178098.1 | 273 | Missense Mutation | CTG,GTG | L71V | NP_001171569.1 |
| NM_001770.5 | 273 | Missense Mutation | CTG,GTG | L71V | NP_001761.3 |
| XM_006721103.3 | 273 | Intron | XP_006721166.1 | ||
| XM_011545981.1 | 273 | Missense Mutation | CTG,GTG | L71V | XP_011544283.1 |
| XM_017023893.1 | 273 | Intron | XP_016879382.1 |