ENST00000682424.1:c.446A>T
|
ENSP00000507321.1:p.Glu149Val
|
|
ENST00000299427.12:c.560A>T
MANE Select
|
ENSP00000299427.6:p.Glu187Val
|
|
ENST00000428886.7:n.795A>T
|
|
|
ENST00000436873.7:c.312+199A>T
|
|
|
ENST00000524788.2:n.1719A>T
|
|
|
ENST00000524903.2:n.1835A>T
|
|
|
ENST00000528807.2:n.216A>T
|
|
|
ENST00000530040.2:n.479+257A>T
|
|
|
ENST00000533371.6:c.-170A>T
|
ENSP00000437066.1:n.-170A>T
|
|
ENST00000534644.6:n.508A>T
|
|
|
ENST00000642892.1:c.-170A>T
|
ENSP00000494165.1:n.-170A>T
|
|
ENST00000643439.1:c.*300A>T
|
ENSP00000495849.1:n.*300A>T
|
|
ENST00000643479.1:n.589A>T
|
|
|
ENST00000643516.1:c.395+199A>T
|
|
|
ENST00000644151.1:n.1999A>T
|
|
|
ENST00000644218.1:c.560A>T
|
ENSP00000493574.1:p.Glu187Val
|
|
ENST00000644683.1:c.*13A>T
|
ENSP00000494085.1:n.*13A>T
|
|
ENST00000644810.1:c.281A>T
|
ENSP00000495895.1:p.Glu94Val
|
|
ENST00000644831.1:n.736A>T
|
|
|
ENST00000644933.1:c.-170A>T
|
ENSP00000496133.1:n.-170A>T
|
|
ENST00000645020.1:n.1735A>T
|
|
|
ENST00000645285.1:c.-170A>T
|
ENSP00000495058.1:n.-170A>T
|
|
ENST00000645331.1:n.926A>T
|
|
|
ENST00000645620.1:c.-170A>T
|
ENSP00000493657.1:n.-170A>T
|
|
ENST00000646777.1:n.736A>T
|
|
|
ENST00000647016.1:n.1040A>T
|
|
|
ENST00000647152.1:c.-170A>T
|
ENSP00000495893.1:n.-170A>T
|
|
ENST00000647209.1:c.*429A>T
|
ENSP00000495558.1:n.*429A>T
|
|
ENST00000647346.1:n.1580A>T
|
|
|
ENST00000299427.10:c.560A>T
|
ENSP00000299427.6:p.Glu187Val
|
|
ENST00000428886.6:n.729A>T
|
|
|
ENST00000436873.6:c.450+257A>T
|
ENSP00000398136.2:n.450+257A>T
|
|
ENST00000524788.1:n.260A>T
|
|
|
ENST00000528571.5:c.*300A>T
|
ENSP00000434647.1:n.*300A>T
|
|
ENST00000528807.1:n.110A>T
|
|
|
ENST00000533371.5:c.-170A>T
|
ENSP00000437066.1:n.-170A>T
|
|
ENST00000534644.5:n.545A>T
|
|
|
ENST00000611494.4:c.560A>T
|
ENSP00000484546.1:p.Glu187Val
|
|
NM_000391.3:c.560A>T
|
NP_000382.3:p.Glu187Val
|
|
NM_000391.4:c.560A>T
MANE Select
|
NP_000382.3:p.Glu187Val
|
|