| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267721.1 | 1053 | Missense Mutation | CCG,CGG | P228R | NP_001254650.1 |
| NM_144603.3 | 1053 | Missense Mutation | CCG,CGG | P223R | NP_653204.1 |
| NM_172167.2 | 1053 | Missense Mutation | CCG,CGG | P224R | NP_751907.1 |
| NM_172168.2 | 1053 | Missense Mutation | CCG,CGG | P229R | NP_751908.1 |
| XM_005255099.4 | 1053 | Missense Mutation | CCG,CGG | P229R | XP_005255156.1 |
| XM_017022927.1 | 1053 | Missense Mutation | CCG,CGG | P229R | XP_016878416.1 |
| XM_017022928.1 | 1053 | Missense Mutation | CCG,CGG | P229R | XP_016878417.1 |