Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182500.2 | 448 | Silent Mutation | CGG,GGG | R56G | NP_872306.1 |
XM_006711857.2 | 448 | Missense Mutation | CGG,GGG | R56G | XP_006711920.1 |
XM_006711858.2 | 448 | Missense Mutation | CGG,GGG | R56G | XP_006711921.1 |
XM_006711859.3 | 448 | Missense Mutation | CGG,GGG | R56G | XP_006711922.1 |