| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032861.3 | 1774 | Silent Mutation | CTA,CTG | L569L | NP_116250.3 |
| XM_006715586.2 | 1774 | Silent Mutation | CTA,CTG | L499L | XP_006715649.1 |
| XM_011536196.2 | 1774 | Silent Mutation | CTA,CTG | L562L | XP_011534498.1 |
| XM_011536198.2 | 1774 | Silent Mutation | CTA,CTG | L499L | XP_011534500.1 |