Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256678.1 | 676 | Missense Mutation | CAA,GAA | Q99E | NP_001243607.1 |
NM_001256679.1 | 676 | Missense Mutation | CAA,GAA | Q4E | NP_001243608.1 |
NM_001256680.1 | 676 | Intron | NP_001243609.1 | ||
NM_001256681.1 | 676 | Intron | NP_001243610.1 | ||
NM_014672.3 | 676 | Missense Mutation | CAA,GAA | Q99E | NP_055487.2 |
XM_005268237.3 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_005268294.1 |
XM_011537409.2 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_011535711.1 |
XM_011537410.2 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_011535712.1 |
XM_017021835.1 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_016877324.1 |
XM_017021836.1 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_016877325.1 |
XM_017021837.1 | 676 | Missense Mutation | CAA,GAA | Q99E | XP_016877326.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001305155.1 | 676 | Intron | NP_001292084.1 | ||
NM_001305156.1 | 676 | Intron | NP_001292085.1 | ||
NM_017917.3 | 676 | Intron | NP_060387.2 | ||
XM_005267782.3 | 676 | Intron | XP_005267839.1 | ||
XM_017021388.1 | 676 | Intron | XP_016876877.1 | ||
XM_017021389.1 | 676 | Intron | XP_016876878.1 |