ENST00000461574.2:c.4182T=
|
ENSP00000417241.2:p.Thr1394=
|
|
ENST00000470026.6:c.4182T=
|
ENSP00000419274.2:p.Thr1394=
|
|
ENST00000473961.6:c.4056T=
|
ENSP00000420201.2:p.Thr1352=
|
|
ENST00000476777.6:c.4179T=
|
ENSP00000417554.2:p.Thr1393=
|
|
ENST00000477152.6:c.4104T=
|
ENSP00000419988.2:p.Thr1368=
|
|
ENST00000478531.6:c.870T=
|
ENSP00000420412.2:p.Thr290=
|
|
ENST00000489037.2:c.4104T=
|
ENSP00000420781.2:p.Thr1368=
|
|
ENST00000493919.6:c.732T=
|
ENSP00000418819.2:p.Thr244=
|
|
ENST00000494123.6:c.4182T=
|
ENSP00000419103.2:p.Thr1394=
|
|
ENST00000497488.2:c.3294T=
|
ENSP00000418986.2:p.Thr1098=
|
|
ENST00000618469.2:c.4182T=
|
ENSP00000478114.2:p.Thr1394=
|
|
ENST00000634433.2:c.4059T=
|
ENSP00000489431.2:p.Thr1353=
|
|
ENST00000644379.2:c.4182T=
|
ENSP00000496570.2:p.Thr1394=
|
|
ENST00000644555.2:c.732T=
|
ENSP00000494614.2:p.Thr244=
|
|
ENST00000652672.2:c.4041T=
|
ENSP00000498906.2:p.Thr1347=
|
|
ENST00000484087.6:c.750T=
|
ENSP00000419481.2:p.Thr250=
|
|
ENST00000700182.1:c.792T=
|
ENSP00000514849.1:p.Thr264=
|
|
ENST00000357654.9:c.4182T=
MANE Select
|
ENSP00000350283.3:p.Thr1394=
|
|
ENST00000471181.7:c.4182T=
|
ENSP00000418960.2:p.Thr1394=
|
|
ENST00000644379.1:c.503T=
|
|
|
ENST00000352993.7:c.756T=
|
ENSP00000312236.5:p.Thr252=
|
|
ENST00000357654.7:c.4182T=
|
ENSP00000350283.3:p.Thr1394=
|
|
ENST00000461221.5:c.*3965T=
|
ENSP00000418548.1:n.*3965T=
|
|
ENST00000461574.1:c.476T=
|
|
|
ENST00000468300.5:c.873T=
|
ENSP00000417148.1:p.Thr291=
|
|
ENST00000471181.6:c.4182T=
|
ENSP00000418960.2:p.Thr1394=
|
|
ENST00000478531.5:c.870T=
|
ENSP00000420412.1:p.Thr290=
|
|
ENST00000484087.5:c.495T=
|
ENSP00000419481.1:p.Thr165=
|
|
ENST00000487825.5:c.498T=
|
ENSP00000418212.1:p.Thr166=
|
|
ENST00000491747.6:c.873T=
|
ENSP00000420705.2:p.Thr291=
|
|
ENST00000493795.5:c.4041T=
|
ENSP00000418775.1:p.Thr1347=
|
|
ENST00000493919.5:c.732T=
|
ENSP00000418819.1:p.Thr244=
|
|
ENST00000586385.5:c.5-26996T=
|
ENSP00000465818.1:n.5-26996T=
|
|
ENST00000591534.5:c.-43-16426T=
|
ENSP00000467329.1:n.-43-16426T=
|
|
ENST00000591849.5:c.-99+34324T=
|
ENSP00000465347.1:n.-99+34324T=
|
|
NM_007294.3:c.4182T= , LRG_292t1:c.4182T=
|
NP_009225.1:p.Thr1394=
|
|
NM_007297.3:c.4041T=
|
NP_009228.2:p.Thr1347=
|
|
NM_007298.3:c.873T=
|
NP_009229.2:p.Thr291=
|
|
NM_007299.3:c.873T=
|
NP_009230.2:p.Thr291=
|
|
NM_007300.3:c.4182T=
|
NP_009231.2:p.Thr1394=
|
|
NR_027676.1:n.4318T=
|
|
|
NM_007294.4:c.4182T=
MANE Select
|
NP_009225.1:p.Thr1394=
|
|
NM_007297.4:c.4041T=
|
NP_009228.2:p.Thr1347=
|
|
NM_007299.4:c.873T=
|
NP_009230.2:p.Thr291=
|
|
NM_007300.4:c.4182T=
|
NP_009231.2:p.Thr1394=
|
|
NR_027676.2:n.4359T=
|
|
|