ENST00000264640.9:c.*639A>G
|
ENSP00000466608.2:n.*639A>G
|
|
ENST00000348513.12:c.1077A>G
MANE Select
|
ENSP00000323967.6:p.Glu359=
|
|
ENST00000377808.9:c.*64A>G
|
ENSP00000367039.4:n.*64A>G
|
|
ENST00000400122.8:c.*64A>G
|
ENSP00000411607.2:n.*64A>G
|
|
ENST00000469334.6:n.1675A>G
|
|
|
ENST00000578044.6:c.867A>G
|
ENSP00000464511.1:p.Glu289=
|
|
ENST00000578112.6:c.*874A>G
|
ENSP00000464501.1:n.*874A>G
|
|
ENST00000580419.6:c.*56A>G
|
ENSP00000462475.2:n.*56A>G
|
|
ENST00000642576.1:n.2220A>G
|
|
|
ENST00000643030.1:n.1700A>G
|
|
|
ENST00000643255.1:c.*3141A>G
|
ENSP00000493957.1:n.*3141A>G
|
|
ENST00000643318.1:c.867A>G
|
ENSP00000494771.1:p.Glu289=
|
|
ENST00000643378.1:n.1632A>G
|
|
|
ENST00000643683.1:c.1077A>G
|
ENSP00000496094.1:p.Glu359=
|
|
ENST00000643893.1:n.1370A>G
|
|
|
ENST00000644443.1:n.2965A>G
|
|
|
ENST00000644523.1:n.1123A>G
|
|
|
ENST00000644527.1:c.849A>G
|
ENSP00000493974.1:p.Glu283=
|
|
ENST00000644701.1:c.*64A>G
|
ENSP00000496097.1:n.*64A>G
|
|
ENST00000644909.1:c.*346A>G
|
ENSP00000493649.1:n.*346A>G
|
|
ENST00000645152.1:n.1740A>G
|
|
|
ENST00000645227.1:c.*765A>G
|
ENSP00000495021.1:n.*765A>G
|
|
ENST00000646242.1:n.6989A>G
|
|
|
ENST00000646283.1:c.885A>G
|
ENSP00000494537.1:p.Glu295=
|
|
ENST00000646401.1:n.2443A>G
|
|
|
ENST00000646448.1:n.2351A>G
|
|
|
ENST00000646856.1:c.*953A>G
|
ENSP00000494505.1:n.*953A>G
|
|
ENST00000647294.1:c.*1007A>G
|
ENSP00000494815.1:n.*1007A>G
|
|
ENST00000647508.1:c.972A>G
|
ENSP00000496445.1:p.Glu324=
|
|
ENST00000647515.1:c.*608A>G
|
ENSP00000495857.1:n.*608A>G
|
|
ENST00000348513.10:c.1077A>G
|
ENSP00000323967.6:p.Glu359=
|
|
ENST00000377808.8:c.*64A>G
|
ENSP00000367039.4:n.*64A>G
|
|
ENST00000400122.7:c.*64A>G
|
ENSP00000411607.2:n.*64A>G
|
|
ENST00000431889.6:c.1023A>G
|
ENSP00000445370.1:p.Glu341=
|
|
ENST00000469334.5:n.1664A>G
|
|
|
ENST00000476049.1:c.*1425A>G
|
ENSP00000463483.1:n.*1425A>G
|
|
ENST00000578044.5:c.867A>G
|
ENSP00000464511.1:p.Glu289=
|
|
ENST00000578112.5:c.*874A>G
|
ENSP00000464501.1:n.*874A>G
|
|
ENST00000580419.5:c.972A>G
|
ENSP00000462475.1:p.Glu324=
|
|
NM_003079.4:c.1077A>G
|
NP_003070.3:p.Glu359=
|
|
NM_003079.5:c.1077A>G
MANE Select
|
NP_003070.3:p.Glu359=
|
|