ENST00000264640.9:c.*731A=
|
ENSP00000466608.2:n.*731A=
|
|
ENST00000348513.12:c.1169A=
MANE Select
|
ENSP00000323967.6:p.Glu390=
|
|
ENST00000377808.9:c.*156A=
|
ENSP00000367039.4:n.*156A=
|
|
ENST00000400122.8:c.*156A=
|
ENSP00000411607.2:n.*156A=
|
|
ENST00000469334.6:n.1767A=
|
|
|
ENST00000578044.6:c.959A=
|
ENSP00000464511.1:p.Glu320=
|
|
ENST00000578112.6:c.*966A=
|
ENSP00000464501.1:n.*966A=
|
|
ENST00000580419.6:c.*148A=
|
ENSP00000462475.2:n.*148A=
|
|
ENST00000642576.1:n.2312A=
|
|
|
ENST00000643030.1:n.1792A=
|
|
|
ENST00000643255.1:c.*3233A=
|
ENSP00000493957.1:n.*3233A=
|
|
ENST00000643318.1:c.959A=
|
ENSP00000494771.1:p.Glu320=
|
|
ENST00000643378.1:n.1724A=
|
|
|
ENST00000643683.1:c.1169A=
|
ENSP00000496094.1:p.Glu390=
|
|
ENST00000643893.1:n.1462A=
|
|
|
ENST00000644443.1:n.3057A=
|
|
|
ENST00000644523.1:n.1215A=
|
|
|
ENST00000644527.1:c.941A=
|
ENSP00000493974.1:p.Glu314=
|
|
ENST00000644701.1:c.*156A=
|
ENSP00000496097.1:n.*156A=
|
|
ENST00000644909.1:c.*438A=
|
ENSP00000493649.1:n.*438A=
|
|
ENST00000645152.1:n.1832A=
|
|
|
ENST00000645227.1:c.*857A=
|
ENSP00000495021.1:n.*857A=
|
|
ENST00000646242.1:n.7081A=
|
|
|
ENST00000646283.1:c.977A=
|
ENSP00000494537.1:p.Glu326=
|
|
ENST00000646401.1:n.2535A=
|
|
|
ENST00000646448.1:n.2443A=
|
|
|
ENST00000646856.1:c.*1045A=
|
ENSP00000494505.1:n.*1045A=
|
|
ENST00000647294.1:c.*1099A=
|
ENSP00000494815.1:n.*1099A=
|
|
ENST00000647508.1:c.1064A=
|
ENSP00000496445.1:p.Glu355=
|
|
ENST00000647515.1:c.*700A=
|
ENSP00000495857.1:n.*700A=
|
|
ENST00000348513.10:c.1169A=
|
ENSP00000323967.6:p.Glu390=
|
|
ENST00000377808.8:c.*156A=
|
ENSP00000367039.4:n.*156A=
|
|
ENST00000400122.7:c.*156A=
|
ENSP00000411607.2:n.*156A=
|
|
ENST00000431889.6:c.1115A=
|
ENSP00000445370.1:p.Glu372=
|
|
ENST00000469334.5:n.1756A=
|
|
|
ENST00000476049.1:c.*1517A=
|
ENSP00000463483.1:n.*1517A=
|
|
ENST00000578044.5:c.959A=
|
ENSP00000464511.1:p.Glu320=
|
|
ENST00000578112.5:c.*966A=
|
ENSP00000464501.1:n.*966A=
|
|
ENST00000580419.5:c.1064A=
|
ENSP00000462475.1:p.Glu355=
|
|
NM_003079.4:c.1169A=
|
NP_003070.3:p.Glu390=
|
|
NM_003079.5:c.1169A=
MANE Select
|
NP_003070.3:p.Glu390=
|
|