| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020815.2 | 1054 | Missense Mutation | CGG,CTG | R68L | NP_065866.1 |
| NM_032961.2 | 1054 | Missense Mutation | CGG,CTG | R68L | NP_116586.1 |
| XM_011532150.1 | 1054 | Missense Mutation | CGG,CTG | R68L | XP_011530452.1 |