Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002334.3 | 4813 | Missense Mutation | CGG,GGG | R1834G | NP_002325.2 |
XM_011520103.2 | 4813 | Missense Mutation | CGG,GGG | R1566G | XP_011518405.1 |
XM_011520104.2 | 4813 | Missense Mutation | CGG,GGG | R1089G | XP_011518406.1 |
XM_017017734.1 | 4813 | Intron | XP_016873223.1 |