| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001244926.1 | 315 | Missense Mutation | CCT,TCT | P68S | NP_001231855.1 |
| NM_001322266.1 | 315 | UTR 5 | NP_001309195.1 | ||
| NM_001322267.1 | 315 | UTR 5 | NP_001309196.1 | ||
| NM_004697.4 | 315 | Missense Mutation | CCT,TCT | P69S | NP_004688.2 |