| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142339.2 | 656 | Intron | NP_001135811.1 | ||
| NM_001261443.1 | 656 | Intron | NP_001248372.1 | ||
| NM_001261444.1 | 656 | Intron | NP_001248373.1 | ||
| NM_182978.3 | 656 | Missense Mutation | CCG,CTG | P36L | NP_892023.1 |
| XM_006722324.2 | 656 | Missense Mutation | CCG,CTG | P36L | XP_006722387.1 |