| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001134875.1 | 425 | Missense Mutation | CCT,TCT | P100S | NP_001128347.1 |
| NM_001134876.1 | 425 | Missense Mutation | CCT,TCT | P100S | NP_001128348.1 |
| NM_001134877.1 | 425 | Missense Mutation | CCT,TCT | P59S | NP_001128349.1 |
| NM_001198983.1 | 425 | Missense Mutation | CCT,TCT | P61S | NP_001185912.1 |