| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001042595.2 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001036060.1 |
| NM_001098821.1 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001092291.1 |
| NM_001098822.1 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001092292.1 |
| NM_001098823.1 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001092293.1 |
| NM_001098824.1 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001092294.1 |
| NM_001098825.1 | 334 | Missense Mutation | CCT,GCT | P59A | NP_001092295.1 |