Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300895.1 | 982 | Intron | NP_001287824.1 | ||
NM_001300896.1 | 982 | Intron | NP_001287825.1 | ||
NM_145200.3 | 982 | Intron | NP_660201.1 | ||
XM_005274114.3 | 982 | Intron | XP_005274171.2 | ||
XM_011545181.2 | 982 | Intron | XP_011543483.1 | ||
XM_011545182.2 | 982 | Intron | XP_011543484.1 | ||
XM_011545183.2 | 982 | Intron | XP_011543485.1 | ||
XM_017018025.1 | 982 | Intron | XP_016873514.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_206997.1 | 982 | Missense Mutation | ACG,ATG | T326M | NP_996880.1 |