| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320276.1 | 487 | Missense Mutation | CCG,CTG | P126L | NP_001307205.1 |
| NM_152536.3 | 487 | Missense Mutation | CCG,CTG | P126L | NP_689749.3 |
| XM_011533422.1 | 487 | Missense Mutation | CCG,CTG | P126L | XP_011531724.1 |
| XM_011533423.1 | 487 | Missense Mutation | CCG,CTG | P126L | XP_011531725.1 |