Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005175.3 | 476 | Intron | NP_001005175.3 | ||
XM_017017711.1 | 476 | Intron | XP_016873200.1 | ||
XM_017017712.1 | 476 | Intron | XP_016873201.1 | ||
XM_017017713.1 | 476 | Intron | XP_016873202.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005180.2 | 476 | Missense Mutation | TGT,TTT | C136F | NP_001005180.1 |