| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286055.1 | 1033 | Missense Mutation | CCT,CGT | P259R | NP_001272984.1 |
| NM_001286056.1 | 1033 | Missense Mutation | CCT,CGT | P264R | NP_001272985.1 |
| NM_001839.4 | 1033 | Missense Mutation | CCT,CGT | P305R | NP_001830.1 |
| XM_017000245.1 | 1033 | Missense Mutation | CCT,CGT | P264R | XP_016855734.1 |