ENST00000682424.1:c.1475A>T
|
ENSP00000507321.1:p.Glu492Val
|
|
ENST00000299427.12:c.1589A>T
MANE Select
|
ENSP00000299427.6:p.Glu530Val
|
|
ENST00000524611.2:n.628A>T
|
|
|
ENST00000524924.2:n.709A>T
|
|
|
ENST00000533371.6:c.860A>T
|
ENSP00000437066.1:p.Glu287Val
|
|
ENST00000642892.1:c.860A>T
|
ENSP00000494165.1:p.Glu287Val
|
|
ENST00000643342.1:c.662A>T
|
|
|
ENST00000643439.1:c.*1329A>T
|
ENSP00000495849.1:n.*1329A>T
|
|
ENST00000643479.1:n.1775A>T
|
|
|
ENST00000643516.1:c.1098A>T
|
|
|
ENST00000644218.1:c.1400A>T
|
ENSP00000493574.1:p.Glu467Val
|
|
ENST00000644683.1:c.*1042A>T
|
ENSP00000494085.1:n.*1042A>T
|
|
ENST00000644810.1:c.1310A>T
|
ENSP00000495895.1:p.Glu437Val
|
|
ENST00000644831.1:n.1765A>T
|
|
|
ENST00000644933.1:c.*455A>T
|
ENSP00000496133.1:n.*455A>T
|
|
ENST00000645285.1:c.*455A>T
|
ENSP00000495058.1:n.*455A>T
|
|
ENST00000645331.1:n.2794A>T
|
|
|
ENST00000645620.1:c.860A>T
|
ENSP00000493657.1:p.Glu287Val
|
|
ENST00000646691.1:n.1476A>T
|
|
|
ENST00000646777.1:n.1922A>T
|
|
|
ENST00000647016.1:n.2069A>T
|
|
|
ENST00000647152.1:c.860A>T
|
ENSP00000495893.1:p.Glu287Val
|
|
ENST00000647209.1:c.*1458A>T
|
ENSP00000495558.1:n.*1458A>T
|
|
ENST00000647346.1:n.2609A>T
|
|
|
ENST00000299427.10:c.1589A>T
|
ENSP00000299427.6:p.Glu530Val
|
|
ENST00000524611.1:n.467A>T
|
|
|
ENST00000533371.5:c.860A>T
|
ENSP00000437066.1:p.Glu287Val
|
|
ENST00000611494.4:c.1589A>T
|
ENSP00000484546.1:p.Glu530Val
|
|
NM_000391.3:c.1589A>T
|
NP_000382.3:p.Glu530Val
|
|
NM_000391.4:c.1589A>T
MANE Select
|
NP_000382.3:p.Glu530Val
|
|