| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282352.1 | 2729 | Missense Mutation | CGG,CTG | R295L | NP_001269281.1 |
| NM_030957.3 | 2729 | Missense Mutation | CGG,CTG | R808L | NP_112219.3 |
| XM_006722917.3 | 2729 | Missense Mutation | CGG,CTG | R440L | XP_006722980.1 |
| XM_017027338.1 | 2729 | Missense Mutation | CGG,CTG | R808L | XP_016882827.1 |
| XM_017027339.1 | 2729 | Missense Mutation | CGG,CTG | R331L | XP_016882828.1 |
| XM_017027340.1 | 2729 | Missense Mutation | CGG,CTG | R329L | XP_016882829.1 |