Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321300.1 | 10116 | Intron | NP_001308229.1 | ||
NM_001321301.1 | 10116 | Intron | NP_001308230.1 | ||
NM_001321302.1 | 10116 | Intron | NP_001308231.1 | ||
NM_001321303.1 | 10116 | Intron | NP_001308232.1 | ||
NM_001321304.1 | 10116 | Intron | NP_001308233.1 | ||
NM_001321305.1 | 10116 | UTR 3 | NP_001308234.1 | ||
NM_152392.4 | 10116 | Intron | NP_689605.1 | ||
XM_011532541.2 | 10116 | UTR 3 | XP_011530843.1 | ||
XM_011532543.2 | 10116 | UTR 3 | XP_011530845.1 | ||
XM_011532545.2 | 10116 | UTR 3 | XP_011530847.1 | ||
XM_017003377.1 | 10116 | UTR 3 | XP_016858866.1 | ||
XM_017003378.1 | 10116 | UTR 3 | XP_016858867.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014709.3 | 10116 | Missense Mutation | GCA,GTA | A3365V | NP_055524.3 |