ENST00000682424.1:c.1490G>T
|
ENSP00000507321.1:p.Gly497Val
|
|
ENST00000299427.12:c.1604G>T
MANE Select
|
ENSP00000299427.6:p.Gly535Val
|
|
ENST00000524611.2:n.643G>T
|
|
|
ENST00000524924.2:n.724G>T
|
|
|
ENST00000533371.6:c.875G>T
|
ENSP00000437066.1:p.Gly292Val
|
|
ENST00000642892.1:c.875G>T
|
ENSP00000494165.1:p.Gly292Val
|
|
ENST00000643342.1:c.677G>T
|
|
|
ENST00000643439.1:c.*1344G>T
|
ENSP00000495849.1:n.*1344G>T
|
|
ENST00000643479.1:n.1790G>T
|
|
|
ENST00000643516.1:c.1113G>T
|
|
|
ENST00000644218.1:c.1415G>T
|
ENSP00000493574.1:p.Gly472Val
|
|
ENST00000644683.1:c.*1057G>T
|
ENSP00000494085.1:n.*1057G>T
|
|
ENST00000644810.1:c.1325G>T
|
ENSP00000495895.1:p.Gly442Val
|
|
ENST00000644831.1:n.1780G>T
|
|
|
ENST00000644933.1:c.*470G>T
|
ENSP00000496133.1:n.*470G>T
|
|
ENST00000645285.1:c.*470G>T
|
ENSP00000495058.1:n.*470G>T
|
|
ENST00000645331.1:n.2809G>T
|
|
|
ENST00000645620.1:c.875G>T
|
ENSP00000493657.1:p.Gly292Val
|
|
ENST00000646691.1:n.1491G>T
|
|
|
ENST00000646777.1:n.1937G>T
|
|
|
ENST00000647016.1:n.2084G>T
|
|
|
ENST00000647152.1:c.875G>T
|
ENSP00000495893.1:p.Gly292Val
|
|
ENST00000647209.1:c.*1473G>T
|
ENSP00000495558.1:n.*1473G>T
|
|
ENST00000647346.1:n.2624G>T
|
|
|
ENST00000299427.10:c.1604G>T
|
ENSP00000299427.6:p.Gly535Val
|
|
ENST00000533371.5:c.875G>T
|
ENSP00000437066.1:p.Gly292Val
|
|
ENST00000611494.4:c.1604G>T
|
ENSP00000484546.1:p.Gly535Val
|
|
NM_000391.3:c.1604G>T
|
NP_000382.3:p.Gly535Val
|
|
NM_000391.4:c.1604G>T
MANE Select
|
NP_000382.3:p.Gly535Val
|
|