Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006764.4 | 1624 | Missense Mutation | CGG,TGG | R499W | NP_006755.4 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304385.1 | 1624 | Intron | NP_001291314.1 | ||
NM_153215.2 | 1624 | Intron | NP_694947.1 | ||
XM_006712979.3 | 1624 | Intron | XP_006713042.1 | ||
XM_006712980.3 | 1624 | Intron | XP_006713043.1 | ||
XM_011533370.2 | 1624 | Intron | XP_011531672.1 |