|
ENST00000509514.6:c.571A=
|
ENSP00000426272.2:p.Thr191=
|
|
|
ENST00000518349.6:c.113-17573A=
|
ENSP00000507185.1:n.113-17573A=
|
|
|
ENST00000682445.1:c.*452A=
|
ENSP00000508061.1:n.*452A=
|
|
|
ENST00000682531.1:n.672A=
|
|
|
|
ENST00000682626.1:c.*77A=
|
ENSP00000507857.1:n.*77A=
|
|
|
ENST00000682996.1:c.571A=
|
ENSP00000507792.1:p.Thr191=
|
|
|
ENST00000683265.1:n.664A=
|
|
|
|
ENST00000683371.1:c.*701A=
|
ENSP00000508376.1:n.*701A=
|
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|
ENST00000683390.1:n.2261A=
|
|
|
|
ENST00000683549.1:n.492A=
|
|
|
|
ENST00000683936.1:c.*456A=
|
ENSP00000507721.1:n.*456A=
|
|
|
ENST00000683974.1:n.653A=
|
|
|
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ENST00000683996.1:c.160A=
|
ENSP00000507060.1:p.Thr54=
|
|
|
ENST00000684131.1:n.410A=
|
|
|
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ENST00000684160.1:c.*261A=
|
ENSP00000507821.1:n.*261A=
|
|
|
ENST00000684214.1:c.571A=
|
ENSP00000508071.1:p.Thr191=
|
|
|
ENST00000414835.7:c.646A=
|
ENSP00000411960.3:p.Thr216=
|
|
|
ENST00000510025.7:c.571A=
MANE Select
|
ENSP00000424940.3:p.Thr191=
|
|
|
ENST00000643250.1:c.*443A=
|
ENSP00000494737.1:n.*443A=
|
|
|
ENST00000644146.1:c.*149A=
|
ENSP00000494808.1:n.*149A=
|
|
|
ENST00000645099.1:c.130A=
|
ENSP00000496091.1:p.Thr44=
|
|
|
ENST00000645702.1:c.160A=
|
ENSP00000496432.1:p.Thr54=
|
|
|
ENST00000645832.1:c.*456A=
|
ENSP00000494316.1:n.*456A=
|
|
|
ENST00000646058.1:c.571A=
|
ENSP00000493579.1:p.Thr191=
|
|
|
ENST00000646355.1:c.*577A=
|
ENSP00000493801.1:n.*577A=
|
|
|
ENST00000646554.1:c.*549A=
|
ENSP00000494542.1:n.*549A=
|
|
|
ENST00000647335.1:c.*538A=
|
ENSP00000495180.1:n.*538A=
|
|
|
ENST00000647342.1:c.*502A=
|
ENSP00000494992.1:n.*502A=
|
|
|
ENST00000256216.10:c.571A=
|
ENSP00000256216.6:p.Thr191=
|
|
|
ENST00000414835.6:c.151A=
|
ENSP00000411960.2:p.Thr51=
|
|
|
ENST00000442060.7:c.571A=
|
ENSP00000390208.3:p.Thr191=
|
|
|
ENST00000503168.5:n.560A=
|
|
|
|
ENST00000504811.5:c.646A=
|
ENSP00000420914.1:p.Thr216=
|
|
|
ENST00000505181.5:n.274A=
|
|
|
|
ENST00000509514.5:c.-314A=
|
ENSP00000426272.1:n.-314A=
|
|
|
ENST00000510025.5:c.499A=
|
ENSP00000424940.1:p.Thr167=
|
|
|
ENST00000512644.1:n.139A=
|
|
|
|
ENST00000513628.5:c.160A=
|
ENSP00000425993.1:p.Thr54=
|
|
|
ENST00000515235.6:n.631A=
|
|
|
|
ENST00000515320.5:c.517A=
|
ENSP00000424613.1:p.Thr173=
|
|
|
NM_000414.3:c.571A=
|
NP_000405.1:p.Thr191=
|
|
|
NM_001199291.2:c.646A=
|
NP_001186220.1:p.Thr216=
|
|
|
NM_001199292.1:c.517A=
|
NP_001186221.1:p.Thr173=
|
|
|
NM_001292027.1:c.499A=
|
NP_001278956.1:p.Thr167=
|
|
|
NM_001292028.1:c.151A=
|
NP_001278957.1:p.Thr51=
|
|
|
NM_000414.4:c.571A=
MANE Select
|
NP_000405.1:p.Thr191=
|
|
|
NM_001199291.3:c.646A=
|
NP_001186220.1:p.Thr216=
|
|
|
NM_001199292.2:c.517A=
|
NP_001186221.1:p.Thr173=
|
|
|
NM_001292027.2:c.499A=
|
NP_001278956.1:p.Thr167=
|
|
|
NM_001292028.2:c.151A=
|
NP_001278957.1:p.Thr51=
|
|
|
NM_001374497.1:c.562A=
|
NP_001361426.1:p.Thr188=
|
|
|
NM_001374498.1:c.571A=
|
NP_001361427.1:p.Thr191=
|
|
|
NM_001374499.1:c.244A=
|
NP_001361428.1:p.Thr82=
|
|
|
NM_001374500.1:c.130A=
|
NP_001361429.1:p.Thr44=
|
|
|
NM_001374501.1:c.160A=
|
NP_001361430.1:p.Thr54=
|
|
|
NM_001374502.1:c.160A=
|
NP_001361431.1:p.Thr54=
|
|
|
NM_001374503.1:c.160A=
|
NP_001361432.1:p.Thr54=
|
|
|
NR_164653.1:n.650A=
|
|
|
|
NR_164654.1:n.838A=
|
|
|
