| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286139.1 | 1355 | Silent Mutation | GCC,GCT | A269A | NP_001273068.1 |
| NM_152313.3 | 1355 | Silent Mutation | GCC,GCT | A404A | NP_689526.2 |
| XM_017017174.1 | 1355 | Missense Mutation | CCG,CTG | P400L | XP_016872663.1 |
| XM_017017175.1 | 1355 | Silent Mutation | GCC,GCT | A298A | XP_016872664.1 |
| XM_017017176.1 | 1355 | Silent Mutation | GCC,GCT | A269A | XP_016872665.1 |
| XM_017017177.1 | 1355 | Missense Mutation | CCG,CTG | P265L | XP_016872666.1 |