ENST00000682424.1:c.1456G>A
|
ENSP00000507321.1:p.Glu486Lys
|
|
ENST00000299427.12:c.1570G>A
MANE Select
|
ENSP00000299427.6:p.Glu524Lys
|
|
ENST00000524611.2:n.609G>A
|
|
|
ENST00000524924.2:n.690G>A
|
|
|
ENST00000533371.6:c.841G>A
|
ENSP00000437066.1:p.Glu281Lys
|
|
ENST00000642892.1:c.841G>A
|
ENSP00000494165.1:p.Glu281Lys
|
|
ENST00000643342.1:c.643G>A
|
|
|
ENST00000643439.1:c.*1310G>A
|
ENSP00000495849.1:n.*1310G>A
|
|
ENST00000643479.1:n.1756G>A
|
|
|
ENST00000643516.1:c.1079G>A
|
|
|
ENST00000644218.1:c.1381G>A
|
ENSP00000493574.1:p.Glu461Lys
|
|
ENST00000644683.1:c.*1023G>A
|
ENSP00000494085.1:n.*1023G>A
|
|
ENST00000644810.1:c.1291G>A
|
ENSP00000495895.1:p.Glu431Lys
|
|
ENST00000644831.1:n.1746G>A
|
|
|
ENST00000644933.1:c.*436G>A
|
ENSP00000496133.1:n.*436G>A
|
|
ENST00000645285.1:c.*436G>A
|
ENSP00000495058.1:n.*436G>A
|
|
ENST00000645331.1:n.2775G>A
|
|
|
ENST00000645620.1:c.841G>A
|
ENSP00000493657.1:p.Glu281Lys
|
|
ENST00000646691.1:n.1457G>A
|
|
|
ENST00000646777.1:n.1903G>A
|
|
|
ENST00000647016.1:n.2050G>A
|
|
|
ENST00000647152.1:c.841G>A
|
ENSP00000495893.1:p.Glu281Lys
|
|
ENST00000647209.1:c.*1439G>A
|
ENSP00000495558.1:n.*1439G>A
|
|
ENST00000647346.1:n.2590G>A
|
|
|
ENST00000299427.10:c.1570G>A
|
ENSP00000299427.6:p.Glu524Lys
|
|
ENST00000524611.1:n.448G>A
|
|
|
ENST00000533371.5:c.841G>A
|
ENSP00000437066.1:p.Glu281Lys
|
|
ENST00000611494.4:c.1570G>A
|
ENSP00000484546.1:p.Glu524Lys
|
|
NM_000391.3:c.1570G>A
|
NP_000382.3:p.Glu524Lys
|
|
NM_000391.4:c.1570G>A
MANE Select
|
NP_000382.3:p.Glu524Lys
|
|