ENST00000682424.1:c.445G>T
|
ENSP00000507321.1:p.Glu149Ter
|
|
ENST00000299427.12:c.559G>T
MANE Select
|
ENSP00000299427.6:p.Glu187Ter
|
|
ENST00000428886.7:n.794G>T
|
|
|
ENST00000436873.7:c.312+198G>T
|
|
|
ENST00000524788.2:n.1718G>T
|
|
|
ENST00000524903.2:n.1834G>T
|
|
|
ENST00000528807.2:n.215G>T
|
|
|
ENST00000530040.2:n.479+256G>T
|
|
|
ENST00000533371.6:c.-171G>T
|
ENSP00000437066.1:n.-171G>T
|
|
ENST00000534644.6:n.507G>T
|
|
|
ENST00000642892.1:c.-171G>T
|
ENSP00000494165.1:n.-171G>T
|
|
ENST00000643439.1:c.*299G>T
|
ENSP00000495849.1:n.*299G>T
|
|
ENST00000643479.1:n.588G>T
|
|
|
ENST00000643516.1:c.395+198G>T
|
|
|
ENST00000644151.1:n.1998G>T
|
|
|
ENST00000644218.1:c.559G>T
|
ENSP00000493574.1:p.Glu187Ter
|
|
ENST00000644683.1:c.*12G>T
|
ENSP00000494085.1:n.*12G>T
|
|
ENST00000644810.1:c.280G>T
|
ENSP00000495895.1:p.Glu94Ter
|
|
ENST00000644831.1:n.735G>T
|
|
|
ENST00000644933.1:c.-171G>T
|
ENSP00000496133.1:n.-171G>T
|
|
ENST00000645020.1:n.1734G>T
|
|
|
ENST00000645285.1:c.-171G>T
|
ENSP00000495058.1:n.-171G>T
|
|
ENST00000645331.1:n.925G>T
|
|
|
ENST00000645620.1:c.-171G>T
|
ENSP00000493657.1:n.-171G>T
|
|
ENST00000646777.1:n.735G>T
|
|
|
ENST00000647016.1:n.1039G>T
|
|
|
ENST00000647152.1:c.-171G>T
|
ENSP00000495893.1:n.-171G>T
|
|
ENST00000647209.1:c.*428G>T
|
ENSP00000495558.1:n.*428G>T
|
|
ENST00000647346.1:n.1579G>T
|
|
|
ENST00000299427.10:c.559G>T
|
ENSP00000299427.6:p.Glu187Ter
|
|
ENST00000428886.6:n.728G>T
|
|
|
ENST00000436873.6:c.450+256G>T
|
ENSP00000398136.2:n.450+256G>T
|
|
ENST00000524788.1:n.259G>T
|
|
|
ENST00000528571.5:c.*299G>T
|
ENSP00000434647.1:n.*299G>T
|
|
ENST00000528807.1:n.109G>T
|
|
|
ENST00000533371.5:c.-171G>T
|
ENSP00000437066.1:n.-171G>T
|
|
ENST00000534644.5:n.544G>T
|
|
|
ENST00000611494.4:c.559G>T
|
ENSP00000484546.1:p.Glu187Ter
|
|
NM_000391.3:c.559G>T
|
NP_000382.3:p.Glu187Ter
|
|
NM_000391.4:c.559G>T
MANE Select
|
NP_000382.3:p.Glu187Ter
|
|