Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001159293.1 | 412 | Missense Mutation | GGT,TGT | G78C | NP_001152765.1 |
XM_005259697.3 | 412 | Missense Mutation | GGT,TGT | G78C | XP_005259754.1 |
XM_006722597.3 | 412 | Missense Mutation | GGT,TGT | G78C | XP_006722660.1 |
XM_011527598.2 | 412 | Intron | XP_011525900.1 | ||
XM_011527599.2 | 412 | Intron | XP_011525901.1 | ||
XM_017026116.1 | 412 | Intron | XP_016881605.1 | ||
XM_017026117.1 | 412 | Intron | XP_016881606.1 |