| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014564.4 | 1360 | Missense Mutation | CCT,CGT | P315R | NP_055379.1 |
| NM_178138.5 | 1360 | Missense Mutation | CCT,CGT | P310R | NP_835258.1 |
| XM_005263410.1 | 1360 | Missense Mutation | CCT,CGT | P299R | XP_005263467.1 |
| XM_017015168.1 | 1360 | Missense Mutation | CCT,CGT | P286R | XP_016870657.1 |