ENST00000682424.1:c.915G=
|
ENSP00000507321.1:p.Glu305=
|
|
ENST00000299427.12:c.1029G=
MANE Select
|
ENSP00000299427.6:p.Glu343=
|
|
ENST00000436873.7:c.313-287G=
|
|
|
ENST00000533371.6:c.300G=
|
ENSP00000437066.1:p.Glu100=
|
|
ENST00000642892.1:c.300G=
|
ENSP00000494165.1:p.Glu100=
|
|
ENST00000643342.1:c.119G=
|
|
|
ENST00000643439.1:c.*769G=
|
ENSP00000495849.1:n.*769G=
|
|
ENST00000643479.1:n.1215G=
|
|
|
ENST00000643516.1:c.538G=
|
|
|
ENST00000644218.1:c.887-287G=
|
ENSP00000493574.1:n.887-287G=
|
|
ENST00000644683.1:c.*482G=
|
ENSP00000494085.1:n.*482G=
|
|
ENST00000644810.1:c.750G=
|
ENSP00000495895.1:p.Glu250=
|
|
ENST00000644831.1:n.1205G=
|
|
|
ENST00000644933.1:c.300G=
|
ENSP00000496133.1:p.Glu100=
|
|
ENST00000645285.1:c.158-287G=
|
ENSP00000495058.1:n.158-287G=
|
|
ENST00000645331.1:n.1552G=
|
|
|
ENST00000645620.1:c.300G=
|
ENSP00000493657.1:p.Glu100=
|
|
ENST00000646691.1:n.122G=
|
|
|
ENST00000646777.1:n.1362G=
|
|
|
ENST00000647016.1:n.1509G=
|
|
|
ENST00000647152.1:c.300G=
|
ENSP00000495893.1:p.Glu100=
|
|
ENST00000647209.1:c.*898G=
|
ENSP00000495558.1:n.*898G=
|
|
ENST00000647346.1:n.2049G=
|
|
|
ENST00000299427.10:c.1029G=
|
ENSP00000299427.6:p.Glu343=
|
|
ENST00000533371.5:c.300G=
|
ENSP00000437066.1:p.Glu100=
|
|
ENST00000611494.4:c.1029G=
|
ENSP00000484546.1:p.Glu343=
|
|
NM_000391.3:c.1029G=
|
NP_000382.3:p.Glu343=
|
|
NM_000391.4:c.1029G=
MANE Select
|
NP_000382.3:p.Glu343=
|
|