ENST00000264640.9:c.*780A>T
|
ENSP00000466608.2:n.*780A>T
|
|
ENST00000348513.12:c.1218A>T
MANE Select
|
ENSP00000323967.6:p.Glu406Asp
|
|
ENST00000377808.9:c.*205A>T
|
ENSP00000367039.4:n.*205A>T
|
|
ENST00000400122.8:c.*205A>T
|
ENSP00000411607.2:n.*205A>T
|
|
ENST00000469334.6:n.1816A>T
|
|
|
ENST00000578044.6:c.1008A>T
|
ENSP00000464511.1:p.Glu336Asp
|
|
ENST00000578112.6:c.*1015A>T
|
ENSP00000464501.1:n.*1015A>T
|
|
ENST00000580419.6:c.*197A>T
|
ENSP00000462475.2:n.*197A>T
|
|
ENST00000642576.1:n.2361A>T
|
|
|
ENST00000643030.1:n.1841A>T
|
|
|
ENST00000643255.1:c.*3282A>T
|
ENSP00000493957.1:n.*3282A>T
|
|
ENST00000643318.1:c.1008A>T
|
ENSP00000494771.1:p.Glu336Asp
|
|
ENST00000643378.1:n.1773A>T
|
|
|
ENST00000643683.1:c.1218A>T
|
ENSP00000496094.1:p.Glu406Asp
|
|
ENST00000643893.1:n.1511A>T
|
|
|
ENST00000644443.1:n.3106A>T
|
|
|
ENST00000644523.1:n.1264A>T
|
|
|
ENST00000644527.1:c.990A>T
|
ENSP00000493974.1:p.Glu330Asp
|
|
ENST00000644701.1:c.*205A>T
|
ENSP00000496097.1:n.*205A>T
|
|
ENST00000644909.1:c.*487A>T
|
ENSP00000493649.1:n.*487A>T
|
|
ENST00000645152.1:n.1881A>T
|
|
|
ENST00000645227.1:c.*906A>T
|
ENSP00000495021.1:n.*906A>T
|
|
ENST00000646242.1:n.7130A>T
|
|
|
ENST00000646283.1:c.1026A>T
|
ENSP00000494537.1:p.Glu342Asp
|
|
ENST00000646401.1:n.2584A>T
|
|
|
ENST00000646448.1:n.2492A>T
|
|
|
ENST00000646856.1:c.*1094A>T
|
ENSP00000494505.1:n.*1094A>T
|
|
ENST00000647294.1:c.*1148A>T
|
ENSP00000494815.1:n.*1148A>T
|
|
ENST00000647508.1:c.1113A>T
|
ENSP00000496445.1:p.Glu371Asp
|
|
ENST00000647515.1:c.*749A>T
|
ENSP00000495857.1:n.*749A>T
|
|
ENST00000348513.10:c.1218A>T
|
ENSP00000323967.6:p.Glu406Asp
|
|
ENST00000377808.8:c.*205A>T
|
ENSP00000367039.4:n.*205A>T
|
|
ENST00000400122.7:c.*205A>T
|
ENSP00000411607.2:n.*205A>T
|
|
ENST00000431889.6:c.1164A>T
|
ENSP00000445370.1:p.Glu388Asp
|
|
ENST00000469334.5:n.1805A>T
|
|
|
ENST00000476049.1:c.*1566A>T
|
ENSP00000463483.1:n.*1566A>T
|
|
ENST00000578044.5:c.1008A>T
|
ENSP00000464511.1:p.Glu336Asp
|
|
ENST00000578112.5:c.*1015A>T
|
ENSP00000464501.1:n.*1015A>T
|
|
ENST00000580419.5:c.1113A>T
|
ENSP00000462475.1:p.Glu371Asp
|
|
NM_003079.4:c.1218A>T
|
NP_003070.3:p.Glu406Asp
|
|
NM_003079.5:c.1218A>T
MANE Select
|
NP_003070.3:p.Glu406Asp
|
|