ENST00000682424.1:c.1458G>C
|
ENSP00000507321.1:p.Glu486Asp
|
|
ENST00000299427.12:c.1572G>C
MANE Select
|
ENSP00000299427.6:p.Glu524Asp
|
|
ENST00000524611.2:n.611G>C
|
|
|
ENST00000524924.2:n.692G>C
|
|
|
ENST00000533371.6:c.843G>C
|
ENSP00000437066.1:p.Glu281Asp
|
|
ENST00000642892.1:c.843G>C
|
ENSP00000494165.1:p.Glu281Asp
|
|
ENST00000643342.1:c.645G>C
|
|
|
ENST00000643439.1:c.*1312G>C
|
ENSP00000495849.1:n.*1312G>C
|
|
ENST00000643479.1:n.1758G>C
|
|
|
ENST00000643516.1:c.1081G>C
|
|
|
ENST00000644218.1:c.1383G>C
|
ENSP00000493574.1:p.Glu461Asp
|
|
ENST00000644683.1:c.*1025G>C
|
ENSP00000494085.1:n.*1025G>C
|
|
ENST00000644810.1:c.1293G>C
|
ENSP00000495895.1:p.Glu431Asp
|
|
ENST00000644831.1:n.1748G>C
|
|
|
ENST00000644933.1:c.*438G>C
|
ENSP00000496133.1:n.*438G>C
|
|
ENST00000645285.1:c.*438G>C
|
ENSP00000495058.1:n.*438G>C
|
|
ENST00000645331.1:n.2777G>C
|
|
|
ENST00000645620.1:c.843G>C
|
ENSP00000493657.1:p.Glu281Asp
|
|
ENST00000646691.1:n.1459G>C
|
|
|
ENST00000646777.1:n.1905G>C
|
|
|
ENST00000647016.1:n.2052G>C
|
|
|
ENST00000647152.1:c.843G>C
|
ENSP00000495893.1:p.Glu281Asp
|
|
ENST00000647209.1:c.*1441G>C
|
ENSP00000495558.1:n.*1441G>C
|
|
ENST00000647346.1:n.2592G>C
|
|
|
ENST00000299427.10:c.1572G>C
|
ENSP00000299427.6:p.Glu524Asp
|
|
ENST00000524611.1:n.450G>C
|
|
|
ENST00000533371.5:c.843G>C
|
ENSP00000437066.1:p.Glu281Asp
|
|
ENST00000611494.4:c.1572G>C
|
ENSP00000484546.1:p.Glu524Asp
|
|
NM_000391.3:c.1572G>C
|
NP_000382.3:p.Glu524Asp
|
|
NM_000391.4:c.1572G>C
MANE Select
|
NP_000382.3:p.Glu524Asp
|
|