|
ENST00000509514.6:c.588G>T
|
ENSP00000426272.2:p.Ala196=
|
|
|
ENST00000518349.6:c.113-17556G>T
|
ENSP00000507185.1:n.113-17556G>T
|
|
|
ENST00000682445.1:c.*469G>T
|
ENSP00000508061.1:n.*469G>T
|
|
|
ENST00000682531.1:n.689G>T
|
|
|
|
ENST00000682626.1:c.*94G>T
|
ENSP00000507857.1:n.*94G>T
|
|
|
ENST00000682996.1:c.588G>T
|
ENSP00000507792.1:p.Ala196=
|
|
|
ENST00000683265.1:n.681G>T
|
|
|
|
ENST00000683371.1:c.*718G>T
|
ENSP00000508376.1:n.*718G>T
|
|
|
ENST00000683390.1:n.2278G>T
|
|
|
|
ENST00000683549.1:n.509G>T
|
|
|
|
ENST00000683936.1:c.*473G>T
|
ENSP00000507721.1:n.*473G>T
|
|
|
ENST00000683974.1:n.670G>T
|
|
|
|
ENST00000683996.1:c.177G>T
|
ENSP00000507060.1:p.Ala59=
|
|
|
ENST00000684131.1:n.427G>T
|
|
|
|
ENST00000684160.1:c.*278G>T
|
ENSP00000507821.1:n.*278G>T
|
|
|
ENST00000684214.1:c.588G>T
|
ENSP00000508071.1:p.Ala196=
|
|
|
ENST00000414835.7:c.663G>T
|
ENSP00000411960.3:p.Ala221=
|
|
|
ENST00000510025.7:c.588G>T
MANE Select
|
ENSP00000424940.3:p.Ala196=
|
|
|
ENST00000643250.1:c.*460G>T
|
ENSP00000494737.1:n.*460G>T
|
|
|
ENST00000644146.1:c.*166G>T
|
ENSP00000494808.1:n.*166G>T
|
|
|
ENST00000645099.1:c.147G>T
|
ENSP00000496091.1:p.Ala49=
|
|
|
ENST00000645702.1:c.177G>T
|
ENSP00000496432.1:p.Ala59=
|
|
|
ENST00000645832.1:c.*473G>T
|
ENSP00000494316.1:n.*473G>T
|
|
|
ENST00000646058.1:c.588G>T
|
ENSP00000493579.1:p.Ala196=
|
|
|
ENST00000646355.1:c.*594G>T
|
ENSP00000493801.1:n.*594G>T
|
|
|
ENST00000646554.1:c.*566G>T
|
ENSP00000494542.1:n.*566G>T
|
|
|
ENST00000647335.1:c.*555G>T
|
ENSP00000495180.1:n.*555G>T
|
|
|
ENST00000647342.1:c.*519G>T
|
ENSP00000494992.1:n.*519G>T
|
|
|
ENST00000256216.10:c.588G>T
|
ENSP00000256216.6:p.Ala196=
|
|
|
ENST00000414835.6:c.168G>T
|
ENSP00000411960.2:p.Ala56=
|
|
|
ENST00000442060.7:c.588G>T
|
ENSP00000390208.3:p.Ala196=
|
|
|
ENST00000503168.5:n.577G>T
|
|
|
|
ENST00000504811.5:c.663G>T
|
ENSP00000420914.1:p.Ala221=
|
|
|
ENST00000505181.5:n.291G>T
|
|
|
|
ENST00000509514.5:c.-297G>T
|
ENSP00000426272.1:n.-297G>T
|
|
|
ENST00000510025.5:c.516G>T
|
ENSP00000424940.1:p.Ala172=
|
|
|
ENST00000512644.1:n.156G>T
|
|
|
|
ENST00000513628.5:c.177G>T
|
ENSP00000425993.1:p.Ala59=
|
|
|
ENST00000515235.6:n.648G>T
|
|
|
|
ENST00000515320.5:c.534G>T
|
ENSP00000424613.1:p.Ala178=
|
|
|
NM_000414.3:c.588G>T
|
NP_000405.1:p.Ala196=
|
|
|
NM_001199291.2:c.663G>T
|
NP_001186220.1:p.Ala221=
|
|
|
NM_001199292.1:c.534G>T
|
NP_001186221.1:p.Ala178=
|
|
|
NM_001292027.1:c.516G>T
|
NP_001278956.1:p.Ala172=
|
|
|
NM_001292028.1:c.168G>T
|
NP_001278957.1:p.Ala56=
|
|
|
NM_000414.4:c.588G>T
MANE Select
|
NP_000405.1:p.Ala196=
|
|
|
NM_001199291.3:c.663G>T
|
NP_001186220.1:p.Ala221=
|
|
|
NM_001199292.2:c.534G>T
|
NP_001186221.1:p.Ala178=
|
|
|
NM_001292027.2:c.516G>T
|
NP_001278956.1:p.Ala172=
|
|
|
NM_001292028.2:c.168G>T
|
NP_001278957.1:p.Ala56=
|
|
|
NM_001374497.1:c.579G>T
|
NP_001361426.1:p.Ala193=
|
|
|
NM_001374498.1:c.588G>T
|
NP_001361427.1:p.Ala196=
|
|
|
NM_001374499.1:c.261G>T
|
NP_001361428.1:p.Ala87=
|
|
|
NM_001374500.1:c.147G>T
|
NP_001361429.1:p.Ala49=
|
|
|
NM_001374501.1:c.177G>T
|
NP_001361430.1:p.Ala59=
|
|
|
NM_001374502.1:c.177G>T
|
NP_001361431.1:p.Ala59=
|
|
|
NM_001374503.1:c.177G>T
|
NP_001361432.1:p.Ala59=
|
|
|
NR_164653.1:n.667G>T
|
|
|
|
NR_164654.1:n.855G>T
|
|
|
