|
ENST00000509514.6:c.456T=
|
ENSP00000426272.2:p.Ala152=
|
|
|
ENST00000518349.6:c.113-17688T=
|
ENSP00000507185.1:n.113-17688T=
|
|
|
ENST00000682445.1:c.*337T=
|
ENSP00000508061.1:n.*337T=
|
|
|
ENST00000682531.1:n.557T=
|
|
|
|
ENST00000682626.1:c.484T=
|
ENSP00000507857.1:p.Phe162=
|
|
|
ENST00000682996.1:c.456T=
|
ENSP00000507792.1:p.Ala152=
|
|
|
ENST00000683265.1:n.549T=
|
|
|
|
ENST00000683371.1:c.*586T=
|
ENSP00000508376.1:n.*586T=
|
|
|
ENST00000683390.1:n.2146T=
|
|
|
|
ENST00000683549.1:n.377T=
|
|
|
|
ENST00000683936.1:c.*341T=
|
ENSP00000507721.1:n.*341T=
|
|
|
ENST00000683974.1:n.538T=
|
|
|
|
ENST00000683996.1:c.45T=
|
ENSP00000507060.1:p.Ala15=
|
|
|
ENST00000684131.1:n.295T=
|
|
|
|
ENST00000684160.1:c.*146T=
|
ENSP00000507821.1:n.*146T=
|
|
|
ENST00000684214.1:c.456T=
|
ENSP00000508071.1:p.Ala152=
|
|
|
ENST00000414835.7:c.531T=
|
ENSP00000411960.3:p.Ala177=
|
|
|
ENST00000510025.7:c.456T=
MANE Select
|
ENSP00000424940.3:p.Ala152=
|
|
|
ENST00000643250.1:c.*328T=
|
ENSP00000494737.1:n.*328T=
|
|
|
ENST00000644146.1:c.*34T=
|
ENSP00000494808.1:n.*34T=
|
|
|
ENST00000645099.1:c.15T=
|
ENSP00000496091.1:p.Ala5=
|
|
|
ENST00000645702.1:c.45T=
|
ENSP00000496432.1:p.Ala15=
|
|
|
ENST00000645832.1:c.*341T=
|
ENSP00000494316.1:n.*341T=
|
|
|
ENST00000646058.1:c.456T=
|
ENSP00000493579.1:p.Ala152=
|
|
|
ENST00000646355.1:c.*462T=
|
ENSP00000493801.1:n.*462T=
|
|
|
ENST00000646554.1:c.*434T=
|
ENSP00000494542.1:n.*434T=
|
|
|
ENST00000646590.1:c.447T=
|
ENSP00000494892.1:p.Ala149=
|
|
|
ENST00000647335.1:c.*423T=
|
ENSP00000495180.1:n.*423T=
|
|
|
ENST00000647342.1:c.*387T=
|
ENSP00000494992.1:n.*387T=
|
|
|
ENST00000256216.10:c.456T=
|
ENSP00000256216.6:p.Ala152=
|
|
|
ENST00000414835.6:c.36T=
|
ENSP00000411960.2:p.Ala12=
|
|
|
ENST00000442060.7:c.456T=
|
ENSP00000390208.3:p.Ala152=
|
|
|
ENST00000503168.5:n.445T=
|
|
|
|
ENST00000504811.5:c.531T=
|
ENSP00000420914.1:p.Ala177=
|
|
|
ENST00000505181.5:n.159T=
|
|
|
|
ENST00000508788.5:n.358T=
|
|
|
|
ENST00000509514.5:c.-429T=
|
ENSP00000426272.1:n.-429T=
|
|
|
ENST00000510025.5:c.384T=
|
ENSP00000424940.1:p.Ala128=
|
|
|
ENST00000512644.1:n.24T=
|
|
|
|
ENST00000512841.5:n.504T=
|
|
|
|
ENST00000513628.5:c.45T=
|
ENSP00000425993.1:p.Ala15=
|
|
|
ENST00000515235.6:n.516T=
|
|
|
|
ENST00000515320.5:c.402T=
|
ENSP00000424613.1:p.Ala134=
|
|
|
NM_000414.3:c.456T=
|
NP_000405.1:p.Ala152=
|
|
|
NM_001199291.2:c.531T=
|
NP_001186220.1:p.Ala177=
|
|
|
NM_001199292.1:c.402T=
|
NP_001186221.1:p.Ala134=
|
|
|
NM_001292027.1:c.384T=
|
NP_001278956.1:p.Ala128=
|
|
|
NM_001292028.1:c.36T=
|
NP_001278957.1:p.Ala12=
|
|
|
NM_000414.4:c.456T=
MANE Select
|
NP_000405.1:p.Ala152=
|
|
|
NM_001199291.3:c.531T=
|
NP_001186220.1:p.Ala177=
|
|
|
NM_001199292.2:c.402T=
|
NP_001186221.1:p.Ala134=
|
|
|
NM_001292027.2:c.384T=
|
NP_001278956.1:p.Ala128=
|
|
|
NM_001292028.2:c.36T=
|
NP_001278957.1:p.Ala12=
|
|
|
NM_001374497.1:c.447T=
|
NP_001361426.1:p.Ala149=
|
|
|
NM_001374498.1:c.456T=
|
NP_001361427.1:p.Ala152=
|
|
|
NM_001374499.1:c.129T=
|
NP_001361428.1:p.Ala43=
|
|
|
NM_001374500.1:c.15T=
|
NP_001361429.1:p.Ala5=
|
|
|
NM_001374501.1:c.45T=
|
NP_001361430.1:p.Ala15=
|
|
|
NM_001374502.1:c.45T=
|
NP_001361431.1:p.Ala15=
|
|
|
NM_001374503.1:c.45T=
|
NP_001361432.1:p.Ala15=
|
|
|
NR_164653.1:n.535T=
|
|
|
|
NR_164654.1:n.723T=
|
|
|
