ENST00000682424.1:c.1554G>A
|
ENSP00000507321.1:p.Leu518=
|
|
ENST00000299427.12:c.1668G>A
MANE Select
|
ENSP00000299427.6:p.Leu556=
|
|
ENST00000524611.2:n.707G>A
|
|
|
ENST00000533371.6:c.939G>A
|
ENSP00000437066.1:p.Leu313=
|
|
ENST00000642892.1:c.939G>A
|
ENSP00000494165.1:p.Leu313=
|
|
ENST00000643342.1:c.741G>A
|
|
|
ENST00000643439.1:c.*1408G>A
|
ENSP00000495849.1:n.*1408G>A
|
|
ENST00000643479.1:n.1854G>A
|
|
|
ENST00000643516.1:c.1177G>A
|
|
|
ENST00000644218.1:c.1479G>A
|
ENSP00000493574.1:p.Leu493=
|
|
ENST00000644683.1:c.*1121G>A
|
ENSP00000494085.1:n.*1121G>A
|
|
ENST00000644810.1:c.1389G>A
|
ENSP00000495895.1:p.Leu463=
|
|
ENST00000644831.1:n.1844G>A
|
|
|
ENST00000644933.1:c.*534G>A
|
ENSP00000496133.1:n.*534G>A
|
|
ENST00000645285.1:c.*534G>A
|
ENSP00000495058.1:n.*534G>A
|
|
ENST00000645331.1:n.2873G>A
|
|
|
ENST00000645620.1:c.939G>A
|
ENSP00000493657.1:p.Leu313=
|
|
ENST00000646691.1:n.1555G>A
|
|
|
ENST00000646777.1:n.2001G>A
|
|
|
ENST00000647016.1:n.2148G>A
|
|
|
ENST00000647152.1:c.939G>A
|
ENSP00000495893.1:p.Leu313=
|
|
ENST00000647209.1:c.*1537G>A
|
ENSP00000495558.1:n.*1537G>A
|
|
ENST00000647346.1:n.2688G>A
|
|
|
ENST00000299427.10:c.1668G>A
|
ENSP00000299427.6:p.Leu556=
|
|
ENST00000533371.5:c.939G>A
|
ENSP00000437066.1:p.Leu313=
|
|
ENST00000611494.4:c.1667G>A
|
ENSP00000484546.1:p.Cys556Tyr
|
|
NM_000391.3:c.1668G>A
|
NP_000382.3:p.Leu556=
|
|
NM_000391.4:c.1668G>A
MANE Select
|
NP_000382.3:p.Leu556=
|
|