| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001166345.1 | 658 | Missense Mutation | GCC,GGC | A23G | NP_001159817.1 |
| NM_001166346.1 | 658 | Missense Mutation | GCC,GGC | A132G | NP_001159818.3 |
| NM_199072.4 | 658 | Missense Mutation | GCC,GGC | A132G | NP_951038.1 |