| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171990.2 | 464 | Silent Mutation | CTA,CTG | L26L | NP_001165461.1 |
| NM_001323018.1 | 464 | Intron | NP_001309947.1 | ||
| NM_001323019.1 | 464 | Silent Mutation | CTA,CTG | L26L | NP_001309948.1 |
| NM_001323020.1 | 464 | Intron | NP_001309949.1 | ||
| NM_001323022.1 | 464 | Intron | NP_001309951.1 | ||
| NM_153706.3 | 464 | Silent Mutation | CTA,CTG | L26L | NP_714917.2 |
| XM_005248426.4 | 464 | Intron | XP_005248483.1 | ||
| XM_011543139.2 | 464 | Intron | XP_011541441.1 | ||
| XM_011543140.2 | 464 | Intron | XP_011541442.1 |