Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001508.2 | 1614 | Missense Mutation | ACC,ATC | T382I | NP_001499.1 |
XM_011511021.2 | 1614 | Intron | XP_011509323.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077427.3 | 1614 | UTR 3 | NP_001070895.1 | ||
NM_001321234.1 | 1614 | UTR 3 | NP_001308163.1 | ||
NM_001321235.1 | 1614 | UTR 3 | NP_001308164.1 | ||
NM_144586.6 | 1614 | UTR 3 | NP_653187.3 | ||
XM_011510546.2 | 1614 | UTR 3 | XP_011508848.1 |