ENST00000264640.9:c.*796T>G
|
ENSP00000466608.2:n.*796T>G
|
|
ENST00000348513.12:c.1234T>G
MANE Select
|
ENSP00000323967.6:p.Ter412Glu
|
|
ENST00000377808.9:c.*221T>G
|
ENSP00000367039.4:n.*221T>G
|
|
ENST00000400122.8:c.*221T>G
|
ENSP00000411607.2:n.*221T>G
|
|
ENST00000469334.6:n.1832T>G
|
|
|
ENST00000578044.6:c.1024T>G
|
ENSP00000464511.1:p.Ter342Glu
|
|
ENST00000578112.6:c.*1031T>G
|
ENSP00000464501.1:n.*1031T>G
|
|
ENST00000580419.6:c.*213T>G
|
ENSP00000462475.2:n.*213T>G
|
|
ENST00000642576.1:n.2377T>G
|
|
|
ENST00000643030.1:n.1857T>G
|
|
|
ENST00000643255.1:c.*3298T>G
|
ENSP00000493957.1:n.*3298T>G
|
|
ENST00000643318.1:c.1024T>G
|
ENSP00000494771.1:p.Ter342Glu
|
|
ENST00000643378.1:n.1789T>G
|
|
|
ENST00000643683.1:c.1234T>G
|
ENSP00000496094.1:p.Ter412Glu
|
|
ENST00000643893.1:n.1527T>G
|
|
|
ENST00000644443.1:n.3122T>G
|
|
|
ENST00000644523.1:n.1280T>G
|
|
|
ENST00000644527.1:c.1006T>G
|
ENSP00000493974.1:p.Ter336Glu
|
|
ENST00000644701.1:c.*221T>G
|
ENSP00000496097.1:n.*221T>G
|
|
ENST00000644909.1:c.*503T>G
|
ENSP00000493649.1:n.*503T>G
|
|
ENST00000645152.1:n.1897T>G
|
|
|
ENST00000645227.1:c.*922T>G
|
ENSP00000495021.1:n.*922T>G
|
|
ENST00000646242.1:n.7146T>G
|
|
|
ENST00000646283.1:c.1042T>G
|
ENSP00000494537.1:p.Ter348Glu
|
|
ENST00000646401.1:n.2600T>G
|
|
|
ENST00000646448.1:n.2508T>G
|
|
|
ENST00000646856.1:c.*1110T>G
|
ENSP00000494505.1:n.*1110T>G
|
|
ENST00000647294.1:c.*1164T>G
|
ENSP00000494815.1:n.*1164T>G
|
|
ENST00000647508.1:c.1129T>G
|
ENSP00000496445.1:p.Ter377Glu
|
|
ENST00000647515.1:c.*765T>G
|
ENSP00000495857.1:n.*765T>G
|
|
ENST00000348513.10:c.1234T>G
|
ENSP00000323967.6:p.Ter412Glu
|
|
ENST00000377808.8:c.*221T>G
|
ENSP00000367039.4:n.*221T>G
|
|
ENST00000400122.7:c.*221T>G
|
ENSP00000411607.2:n.*221T>G
|
|
ENST00000431889.6:c.1180T>G
|
ENSP00000445370.1:p.Ter394Glu
|
|
ENST00000469334.5:n.1821T>G
|
|
|
ENST00000578044.5:c.1024T>G
|
ENSP00000464511.1:p.Ter342Glu
|
|
ENST00000578112.5:c.*1031T>G
|
ENSP00000464501.1:n.*1031T>G
|
|
ENST00000580419.5:c.1129T>G
|
ENSP00000462475.1:p.Ter377Glu
|
|
NM_003079.4:c.1234T>G
|
NP_003070.3:p.Ter412Glu
|
|
NM_003079.5:c.1234T>G
MANE Select
|
NP_003070.3:p.Ter412Glu
|
|