ENST00000264640.9:c.*743C>T
|
ENSP00000466608.2:n.*743C>T
|
|
ENST00000348513.12:c.1181C>T
MANE Select
|
ENSP00000323967.6:p.Ala394Val
|
|
ENST00000377808.9:c.*168C>T
|
ENSP00000367039.4:n.*168C>T
|
|
ENST00000400122.8:c.*168C>T
|
ENSP00000411607.2:n.*168C>T
|
|
ENST00000469334.6:n.1779C>T
|
|
|
ENST00000578044.6:c.971C>T
|
ENSP00000464511.1:p.Ala324Val
|
|
ENST00000578112.6:c.*978C>T
|
ENSP00000464501.1:n.*978C>T
|
|
ENST00000580419.6:c.*160C>T
|
ENSP00000462475.2:n.*160C>T
|
|
ENST00000642576.1:n.2324C>T
|
|
|
ENST00000643030.1:n.1804C>T
|
|
|
ENST00000643255.1:c.*3245C>T
|
ENSP00000493957.1:n.*3245C>T
|
|
ENST00000643318.1:c.971C>T
|
ENSP00000494771.1:p.Ala324Val
|
|
ENST00000643378.1:n.1736C>T
|
|
|
ENST00000643683.1:c.1181C>T
|
ENSP00000496094.1:p.Ala394Val
|
|
ENST00000643893.1:n.1474C>T
|
|
|
ENST00000644443.1:n.3069C>T
|
|
|
ENST00000644523.1:n.1227C>T
|
|
|
ENST00000644527.1:c.953C>T
|
ENSP00000493974.1:p.Ala318Val
|
|
ENST00000644701.1:c.*168C>T
|
ENSP00000496097.1:n.*168C>T
|
|
ENST00000644909.1:c.*450C>T
|
ENSP00000493649.1:n.*450C>T
|
|
ENST00000645152.1:n.1844C>T
|
|
|
ENST00000645227.1:c.*869C>T
|
ENSP00000495021.1:n.*869C>T
|
|
ENST00000646242.1:n.7093C>T
|
|
|
ENST00000646283.1:c.989C>T
|
ENSP00000494537.1:p.Ala330Val
|
|
ENST00000646401.1:n.2547C>T
|
|
|
ENST00000646448.1:n.2455C>T
|
|
|
ENST00000646856.1:c.*1057C>T
|
ENSP00000494505.1:n.*1057C>T
|
|
ENST00000647294.1:c.*1111C>T
|
ENSP00000494815.1:n.*1111C>T
|
|
ENST00000647508.1:c.1076C>T
|
ENSP00000496445.1:p.Ala359Val
|
|
ENST00000647515.1:c.*712C>T
|
ENSP00000495857.1:n.*712C>T
|
|
ENST00000348513.10:c.1181C>T
|
ENSP00000323967.6:p.Ala394Val
|
|
ENST00000377808.8:c.*168C>T
|
ENSP00000367039.4:n.*168C>T
|
|
ENST00000400122.7:c.*168C>T
|
ENSP00000411607.2:n.*168C>T
|
|
ENST00000431889.6:c.1127C>T
|
ENSP00000445370.1:p.Ala376Val
|
|
ENST00000469334.5:n.1768C>T
|
|
|
ENST00000476049.1:c.*1529C>T
|
ENSP00000463483.1:n.*1529C>T
|
|
ENST00000578044.5:c.971C>T
|
ENSP00000464511.1:p.Ala324Val
|
|
ENST00000578112.5:c.*978C>T
|
ENSP00000464501.1:n.*978C>T
|
|
ENST00000580419.5:c.1076C>T
|
ENSP00000462475.1:p.Ala359Val
|
|
NM_003079.4:c.1181C>T
|
NP_003070.3:p.Ala394Val
|
|
NM_003079.5:c.1181C>T
MANE Select
|
NP_003070.3:p.Ala394Val
|
|