ENST00000264640.9:c.*782A>T
|
ENSP00000466608.2:n.*782A>T
|
|
ENST00000348513.12:c.1220A>T
MANE Select
|
ENSP00000323967.6:p.Asp407Val
|
|
ENST00000377808.9:c.*207A>T
|
ENSP00000367039.4:n.*207A>T
|
|
ENST00000400122.8:c.*207A>T
|
ENSP00000411607.2:n.*207A>T
|
|
ENST00000469334.6:n.1818A>T
|
|
|
ENST00000578044.6:c.1010A>T
|
ENSP00000464511.1:p.Asp337Val
|
|
ENST00000578112.6:c.*1017A>T
|
ENSP00000464501.1:n.*1017A>T
|
|
ENST00000580419.6:c.*199A>T
|
ENSP00000462475.2:n.*199A>T
|
|
ENST00000642576.1:n.2363A>T
|
|
|
ENST00000643030.1:n.1843A>T
|
|
|
ENST00000643255.1:c.*3284A>T
|
ENSP00000493957.1:n.*3284A>T
|
|
ENST00000643318.1:c.1010A>T
|
ENSP00000494771.1:p.Asp337Val
|
|
ENST00000643378.1:n.1775A>T
|
|
|
ENST00000643683.1:c.1220A>T
|
ENSP00000496094.1:p.Asp407Val
|
|
ENST00000643893.1:n.1513A>T
|
|
|
ENST00000644443.1:n.3108A>T
|
|
|
ENST00000644523.1:n.1266A>T
|
|
|
ENST00000644527.1:c.992A>T
|
ENSP00000493974.1:p.Asp331Val
|
|
ENST00000644701.1:c.*207A>T
|
ENSP00000496097.1:n.*207A>T
|
|
ENST00000644909.1:c.*489A>T
|
ENSP00000493649.1:n.*489A>T
|
|
ENST00000645152.1:n.1883A>T
|
|
|
ENST00000645227.1:c.*908A>T
|
ENSP00000495021.1:n.*908A>T
|
|
ENST00000646242.1:n.7132A>T
|
|
|
ENST00000646283.1:c.1028A>T
|
ENSP00000494537.1:p.Asp343Val
|
|
ENST00000646401.1:n.2586A>T
|
|
|
ENST00000646448.1:n.2494A>T
|
|
|
ENST00000646856.1:c.*1096A>T
|
ENSP00000494505.1:n.*1096A>T
|
|
ENST00000647294.1:c.*1150A>T
|
ENSP00000494815.1:n.*1150A>T
|
|
ENST00000647508.1:c.1115A>T
|
ENSP00000496445.1:p.Asp372Val
|
|
ENST00000647515.1:c.*751A>T
|
ENSP00000495857.1:n.*751A>T
|
|
ENST00000348513.10:c.1220A>T
|
ENSP00000323967.6:p.Asp407Val
|
|
ENST00000377808.8:c.*207A>T
|
ENSP00000367039.4:n.*207A>T
|
|
ENST00000400122.7:c.*207A>T
|
ENSP00000411607.2:n.*207A>T
|
|
ENST00000431889.6:c.1166A>T
|
ENSP00000445370.1:p.Asp389Val
|
|
ENST00000469334.5:n.1807A>T
|
|
|
ENST00000476049.1:c.*1568A>T
|
ENSP00000463483.1:n.*1568A>T
|
|
ENST00000578044.5:c.1010A>T
|
ENSP00000464511.1:p.Asp337Val
|
|
ENST00000578112.5:c.*1017A>T
|
ENSP00000464501.1:n.*1017A>T
|
|
ENST00000580419.5:c.1115A>T
|
ENSP00000462475.1:p.Asp372Val
|
|
NM_003079.4:c.1220A>T
|
NP_003070.3:p.Asp407Val
|
|
NM_003079.5:c.1220A>T
MANE Select
|
NP_003070.3:p.Asp407Val
|
|