| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152706.3 | 666 | Missense Mutation | ACA,GCA | T162A | NP_689919.1 |
| XM_011515904.2 | 666 | Missense Mutation | ACA,GCA | T162A | XP_011514206.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_181646.3 | 666 | Intron | NP_857597.1 |