| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278733.1 | 2238 | Missense Mutation | CCT,GCT | P573A | NP_001265662.1 |
| NM_054114.4 | 2238 | Missense Mutation | CCT,GCT | P636A | NP_473455.2 |
| NM_138810.3 | 2238 | Intron | NP_620165.1 | ||
| NM_152133.2 | 2238 | Missense Mutation | CCT,GCT | P458A | NP_687034.1 |