| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195286.1 | 388 | Missense Mutation | CCG,GCG | P88A | NP_001182215.1 |
| NM_002460.3 | 388 | Missense Mutation | CCG,GCG | P88A | NP_002451.2 |
| XM_006715090.2 | 388 | Missense Mutation | CCG,GCG | P88A | XP_006715153.1 |