ENST00000264640.9:c.*785A>T
|
ENSP00000466608.2:n.*785A>T
|
|
ENST00000348513.12:c.1223A>T
MANE Select
|
ENSP00000323967.6:p.Glu408Val
|
|
ENST00000377808.9:c.*210A>T
|
ENSP00000367039.4:n.*210A>T
|
|
ENST00000400122.8:c.*210A>T
|
ENSP00000411607.2:n.*210A>T
|
|
ENST00000469334.6:n.1821A>T
|
|
|
ENST00000578044.6:c.1013A>T
|
ENSP00000464511.1:p.Glu338Val
|
|
ENST00000578112.6:c.*1020A>T
|
ENSP00000464501.1:n.*1020A>T
|
|
ENST00000580419.6:c.*202A>T
|
ENSP00000462475.2:n.*202A>T
|
|
ENST00000642576.1:n.2366A>T
|
|
|
ENST00000643030.1:n.1846A>T
|
|
|
ENST00000643255.1:c.*3287A>T
|
ENSP00000493957.1:n.*3287A>T
|
|
ENST00000643318.1:c.1013A>T
|
ENSP00000494771.1:p.Glu338Val
|
|
ENST00000643378.1:n.1778A>T
|
|
|
ENST00000643683.1:c.1223A>T
|
ENSP00000496094.1:p.Glu408Val
|
|
ENST00000643893.1:n.1516A>T
|
|
|
ENST00000644443.1:n.3111A>T
|
|
|
ENST00000644523.1:n.1269A>T
|
|
|
ENST00000644527.1:c.995A>T
|
ENSP00000493974.1:p.Glu332Val
|
|
ENST00000644701.1:c.*210A>T
|
ENSP00000496097.1:n.*210A>T
|
|
ENST00000644909.1:c.*492A>T
|
ENSP00000493649.1:n.*492A>T
|
|
ENST00000645152.1:n.1886A>T
|
|
|
ENST00000645227.1:c.*911A>T
|
ENSP00000495021.1:n.*911A>T
|
|
ENST00000646242.1:n.7135A>T
|
|
|
ENST00000646283.1:c.1031A>T
|
ENSP00000494537.1:p.Glu344Val
|
|
ENST00000646401.1:n.2589A>T
|
|
|
ENST00000646448.1:n.2497A>T
|
|
|
ENST00000646856.1:c.*1099A>T
|
ENSP00000494505.1:n.*1099A>T
|
|
ENST00000647294.1:c.*1153A>T
|
ENSP00000494815.1:n.*1153A>T
|
|
ENST00000647508.1:c.1118A>T
|
ENSP00000496445.1:p.Glu373Val
|
|
ENST00000647515.1:c.*754A>T
|
ENSP00000495857.1:n.*754A>T
|
|
ENST00000348513.10:c.1223A>T
|
ENSP00000323967.6:p.Glu408Val
|
|
ENST00000377808.8:c.*210A>T
|
ENSP00000367039.4:n.*210A>T
|
|
ENST00000400122.7:c.*210A>T
|
ENSP00000411607.2:n.*210A>T
|
|
ENST00000431889.6:c.1169A>T
|
ENSP00000445370.1:p.Glu390Val
|
|
ENST00000469334.5:n.1810A>T
|
|
|
ENST00000476049.1:c.*1571A>T
|
ENSP00000463483.1:n.*1571A>T
|
|
ENST00000578044.5:c.1013A>T
|
ENSP00000464511.1:p.Glu338Val
|
|
ENST00000578112.5:c.*1020A>T
|
ENSP00000464501.1:n.*1020A>T
|
|
ENST00000580419.5:c.1118A>T
|
ENSP00000462475.1:p.Glu373Val
|
|
NM_003079.4:c.1223A>T
|
NP_003070.3:p.Glu408Val
|
|
NM_003079.5:c.1223A>T
MANE Select
|
NP_003070.3:p.Glu408Val
|
|