Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033063.1 | 4684 | Missense Mutation | CGG,GGG | R678G | NP_149052.1 |
NM_207577.1 | 4684 | Intron | NP_997460.1 | ||
XM_006718556.3 | 4684 | Intron | XP_006718619.1 | ||
XM_011545039.2 | 4684 | Intron | XP_011543341.1 | ||
XM_017017755.1 | 4684 | Missense Mutation | CGG,GGG | R694G | XP_016873244.1 |
XM_017017756.1 | 4684 | Missense Mutation | CGG,GGG | R393G | XP_016873245.1 |
XM_017017757.1 | 4684 | Missense Mutation | CGG,GGG | R377G | XP_016873246.1 |
XM_017017758.1 | 4684 | Missense Mutation | CGG,GGG | R365G | XP_016873247.1 |