|
ENST00000509514.6:c.466T>A
|
ENSP00000426272.2:p.Tyr156Asn
|
|
|
ENST00000518349.6:c.113-17678T>A
|
ENSP00000507185.1:n.113-17678T>A
|
|
|
ENST00000682445.1:c.*347T>A
|
ENSP00000508061.1:n.*347T>A
|
|
|
ENST00000682531.1:n.567T>A
|
|
|
|
ENST00000682626.1:c.494T>A
|
ENSP00000507857.1:p.Ile165Lys
|
|
|
ENST00000682996.1:c.466T>A
|
ENSP00000507792.1:p.Tyr156Asn
|
|
|
ENST00000683265.1:n.559T>A
|
|
|
|
ENST00000683371.1:c.*596T>A
|
ENSP00000508376.1:n.*596T>A
|
|
|
ENST00000683390.1:n.2156T>A
|
|
|
|
ENST00000683549.1:n.387T>A
|
|
|
|
ENST00000683936.1:c.*351T>A
|
ENSP00000507721.1:n.*351T>A
|
|
|
ENST00000683974.1:n.548T>A
|
|
|
|
ENST00000683996.1:c.55T>A
|
ENSP00000507060.1:p.Tyr19Asn
|
|
|
ENST00000684131.1:n.305T>A
|
|
|
|
ENST00000684160.1:c.*156T>A
|
ENSP00000507821.1:n.*156T>A
|
|
|
ENST00000684214.1:c.466T>A
|
ENSP00000508071.1:p.Tyr156Asn
|
|
|
ENST00000414835.7:c.541T>A
|
ENSP00000411960.3:p.Tyr181Asn
|
|
|
ENST00000510025.7:c.466T>A
MANE Select
|
ENSP00000424940.3:p.Tyr156Asn
|
|
|
ENST00000643250.1:c.*338T>A
|
ENSP00000494737.1:n.*338T>A
|
|
|
ENST00000644146.1:c.*44T>A
|
ENSP00000494808.1:n.*44T>A
|
|
|
ENST00000645099.1:c.25T>A
|
ENSP00000496091.1:p.Tyr9Asn
|
|
|
ENST00000645702.1:c.55T>A
|
ENSP00000496432.1:p.Tyr19Asn
|
|
|
ENST00000645832.1:c.*351T>A
|
ENSP00000494316.1:n.*351T>A
|
|
|
ENST00000646058.1:c.466T>A
|
ENSP00000493579.1:p.Tyr156Asn
|
|
|
ENST00000646355.1:c.*472T>A
|
ENSP00000493801.1:n.*472T>A
|
|
|
ENST00000646554.1:c.*444T>A
|
ENSP00000494542.1:n.*444T>A
|
|
|
ENST00000646590.1:c.457T>A
|
ENSP00000494892.1:p.Tyr153Asn
|
|
|
ENST00000647335.1:c.*433T>A
|
ENSP00000495180.1:n.*433T>A
|
|
|
ENST00000647342.1:c.*397T>A
|
ENSP00000494992.1:n.*397T>A
|
|
|
ENST00000256216.10:c.466T>A
|
ENSP00000256216.6:p.Tyr156Asn
|
|
|
ENST00000414835.6:c.46T>A
|
ENSP00000411960.2:p.Tyr16Asn
|
|
|
ENST00000442060.7:c.466T>A
|
ENSP00000390208.3:p.Tyr156Asn
|
|
|
ENST00000503168.5:n.455T>A
|
|
|
|
ENST00000504811.5:c.541T>A
|
ENSP00000420914.1:p.Tyr181Asn
|
|
|
ENST00000505181.5:n.169T>A
|
|
|
|
ENST00000508788.5:n.368T>A
|
|
|
|
ENST00000509514.5:c.-419T>A
|
ENSP00000426272.1:n.-419T>A
|
|
|
ENST00000510025.5:c.394T>A
|
ENSP00000424940.1:p.Tyr132Asn
|
|
|
ENST00000512644.1:n.34T>A
|
|
|
|
ENST00000512841.5:n.514T>A
|
|
|
|
ENST00000513628.5:c.55T>A
|
ENSP00000425993.1:p.Tyr19Asn
|
|
|
ENST00000515235.6:n.526T>A
|
|
|
|
ENST00000515320.5:c.412T>A
|
ENSP00000424613.1:p.Tyr138Asn
|
|
|
NM_000414.3:c.466T>A
|
NP_000405.1:p.Tyr156Asn
|
|
|
NM_001199291.2:c.541T>A
|
NP_001186220.1:p.Tyr181Asn
|
|
|
NM_001199292.1:c.412T>A
|
NP_001186221.1:p.Tyr138Asn
|
|
|
NM_001292027.1:c.394T>A
|
NP_001278956.1:p.Tyr132Asn
|
|
|
NM_001292028.1:c.46T>A
|
NP_001278957.1:p.Tyr16Asn
|
|
|
NM_000414.4:c.466T>A
MANE Select
|
NP_000405.1:p.Tyr156Asn
|
|
|
NM_001199291.3:c.541T>A
|
NP_001186220.1:p.Tyr181Asn
|
|
|
NM_001199292.2:c.412T>A
|
NP_001186221.1:p.Tyr138Asn
|
|
|
NM_001292027.2:c.394T>A
|
NP_001278956.1:p.Tyr132Asn
|
|
|
NM_001292028.2:c.46T>A
|
NP_001278957.1:p.Tyr16Asn
|
|
|
NM_001374497.1:c.457T>A
|
NP_001361426.1:p.Tyr153Asn
|
|
|
NM_001374498.1:c.466T>A
|
NP_001361427.1:p.Tyr156Asn
|
|
|
NM_001374499.1:c.139T>A
|
NP_001361428.1:p.Tyr47Asn
|
|
|
NM_001374500.1:c.25T>A
|
NP_001361429.1:p.Tyr9Asn
|
|
|
NM_001374501.1:c.55T>A
|
NP_001361430.1:p.Tyr19Asn
|
|
|
NM_001374502.1:c.55T>A
|
NP_001361431.1:p.Tyr19Asn
|
|
|
NM_001374503.1:c.55T>A
|
NP_001361432.1:p.Tyr19Asn
|
|
|
NR_164653.1:n.545T>A
|
|
|
|
NR_164654.1:n.733T>A
|
|
|
