ENST00000264640.9:c.*778G=
|
ENSP00000466608.2:n.*778G=
|
|
ENST00000348513.12:c.1216G=
MANE Select
|
ENSP00000323967.6:p.Glu406=
|
|
ENST00000377808.9:c.*203G=
|
ENSP00000367039.4:n.*203G=
|
|
ENST00000400122.8:c.*203G=
|
ENSP00000411607.2:n.*203G=
|
|
ENST00000469334.6:n.1814G=
|
|
|
ENST00000578044.6:c.1006G=
|
ENSP00000464511.1:p.Glu336=
|
|
ENST00000578112.6:c.*1013G=
|
ENSP00000464501.1:n.*1013G=
|
|
ENST00000580419.6:c.*195G=
|
ENSP00000462475.2:n.*195G=
|
|
ENST00000642576.1:n.2359G=
|
|
|
ENST00000643030.1:n.1839G=
|
|
|
ENST00000643255.1:c.*3280G=
|
ENSP00000493957.1:n.*3280G=
|
|
ENST00000643318.1:c.1006G=
|
ENSP00000494771.1:p.Glu336=
|
|
ENST00000643378.1:n.1771G=
|
|
|
ENST00000643683.1:c.1216G=
|
ENSP00000496094.1:p.Glu406=
|
|
ENST00000643893.1:n.1509G=
|
|
|
ENST00000644443.1:n.3104G=
|
|
|
ENST00000644523.1:n.1262G=
|
|
|
ENST00000644527.1:c.988G=
|
ENSP00000493974.1:p.Glu330=
|
|
ENST00000644701.1:c.*203G=
|
ENSP00000496097.1:n.*203G=
|
|
ENST00000644909.1:c.*485G=
|
ENSP00000493649.1:n.*485G=
|
|
ENST00000645152.1:n.1879G=
|
|
|
ENST00000645227.1:c.*904G=
|
ENSP00000495021.1:n.*904G=
|
|
ENST00000646242.1:n.7128G=
|
|
|
ENST00000646283.1:c.1024G=
|
ENSP00000494537.1:p.Glu342=
|
|
ENST00000646401.1:n.2582G=
|
|
|
ENST00000646448.1:n.2490G=
|
|
|
ENST00000646856.1:c.*1092G=
|
ENSP00000494505.1:n.*1092G=
|
|
ENST00000647294.1:c.*1146G=
|
ENSP00000494815.1:n.*1146G=
|
|
ENST00000647508.1:c.1111G=
|
ENSP00000496445.1:p.Glu371=
|
|
ENST00000647515.1:c.*747G=
|
ENSP00000495857.1:n.*747G=
|
|
ENST00000348513.10:c.1216G=
|
ENSP00000323967.6:p.Glu406=
|
|
ENST00000377808.8:c.*203G=
|
ENSP00000367039.4:n.*203G=
|
|
ENST00000400122.7:c.*203G=
|
ENSP00000411607.2:n.*203G=
|
|
ENST00000431889.6:c.1162G=
|
ENSP00000445370.1:p.Glu388=
|
|
ENST00000469334.5:n.1803G=
|
|
|
ENST00000476049.1:c.*1564G=
|
ENSP00000463483.1:n.*1564G=
|
|
ENST00000578044.5:c.1006G=
|
ENSP00000464511.1:p.Glu336=
|
|
ENST00000578112.5:c.*1013G=
|
ENSP00000464501.1:n.*1013G=
|
|
ENST00000580419.5:c.1111G=
|
ENSP00000462475.1:p.Glu371=
|
|
NM_003079.4:c.1216G=
|
NP_003070.3:p.Glu406=
|
|
NM_003079.5:c.1216G=
MANE Select
|
NP_003070.3:p.Glu406=
|
|