Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004146.5 | 393 | Missense Mutation | CGG,GGG | R106G | NP_004137.2 |
XM_011528039.2 | 393 | Missense Mutation | CGG,GGG | R68G | XP_011526341.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321170.1 | 393 | Intron | NP_001308099.1 | ||
NM_138501.5 | 393 | Intron | NP_612510.1 | ||
XM_006722945.1 | 393 | Intron | XP_006723008.1 | ||
XM_011528442.2 | 393 | Intron | XP_011526744.1 |