Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014805.3 | 292 | Intron | NP_055620.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000249.3 | 292 | Missense Mutation | ATC,GTC | I32V | NP_000240.1 |
NM_001167617.1 | 292 | Intron | NP_001161089.1 | ||
NM_001167618.1 | 292 | Intron | NP_001161090.1 | ||
NM_001167619.1 | 292 | Intron | NP_001161091.1 | ||
NM_001258271.1 | 292 | Missense Mutation | ATC,GTC | I32V | NP_001245200.1 |
NM_001258273.1 | 292 | UTR 5 | NP_001245202.1 | ||
NM_001258274.1 | 292 | Intron | NP_001245203.1 | ||
XM_005265161.1 | 292 | Missense Mutation | ATC,GTC | I32V | XP_005265218.1 |
XM_005265163.1 | 292 | Intron | XP_005265220.1 | ||
XM_005265164.1 | 292 | UTR 5 | XP_005265221.1 | ||
XM_005265166.1 | 292 | Intron | XP_005265223.1 | ||
XM_011533727.1 | 292 | Intron | XP_011532029.1 | ||
XM_017006449.1 | 292 | Intron | XP_016861938.1 | ||
XM_017006450.1 | 292 | UTR 5 | XP_016861939.1 | ||
XM_017006451.1 | 292 | UTR 5 | XP_016861940.1 |