| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304347.1 | 722 | Missense Mutation | ACC,GCC | T212A | NP_001291276.1 |
| NM_001304348.1 | 722 | Missense Mutation | ACC,GCC | T110A | NP_001291277.1 |
| NM_058164.3 | 722 | Missense Mutation | ACC,GCC | T188A | NP_477512.1 |