Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144616.3 | 740 | Missense Mutation | GCC,GTC | A92V | NP_653217.1 |
XM_017026285.1 | 740 | Missense Mutation | GCC,GTC | A138V | XP_016881774.1 |
XM_017026286.1 | 740 | Missense Mutation | GCC,GTC | A138V | XP_016881775.1 |
XM_017026287.1 | 740 | Missense Mutation | GCC,GTC | A92V | XP_016881776.1 |