ENST00000682424.1:c.483G>A
|
ENSP00000507321.1:p.Gly161=
|
|
ENST00000299427.12:c.597G>A
MANE Select
|
ENSP00000299427.6:p.Gly199=
|
|
ENST00000428886.7:n.832G>A
|
|
|
ENST00000436873.7:c.312+236G>A
|
|
|
ENST00000524788.2:n.1756G>A
|
|
|
ENST00000524903.2:n.1872G>A
|
|
|
ENST00000528807.2:n.253G>A
|
|
|
ENST00000530040.2:n.479+294G>A
|
|
|
ENST00000533371.6:c.-133G>A
|
ENSP00000437066.1:n.-133G>A
|
|
ENST00000534644.6:n.545G>A
|
|
|
ENST00000642892.1:c.-133G>A
|
ENSP00000494165.1:n.-133G>A
|
|
ENST00000643439.1:c.*337G>A
|
ENSP00000495849.1:n.*337G>A
|
|
ENST00000643479.1:n.626G>A
|
|
|
ENST00000643516.1:c.395+236G>A
|
|
|
ENST00000644151.1:n.2036G>A
|
|
|
ENST00000644218.1:c.597G>A
|
ENSP00000493574.1:p.Gly199=
|
|
ENST00000644683.1:c.*50G>A
|
ENSP00000494085.1:n.*50G>A
|
|
ENST00000644810.1:c.318G>A
|
ENSP00000495895.1:p.Gly106=
|
|
ENST00000644831.1:n.773G>A
|
|
|
ENST00000644933.1:c.-133G>A
|
ENSP00000496133.1:n.-133G>A
|
|
ENST00000645020.1:n.1772G>A
|
|
|
ENST00000645285.1:c.-133G>A
|
ENSP00000495058.1:n.-133G>A
|
|
ENST00000645331.1:n.963G>A
|
|
|
ENST00000645620.1:c.-133G>A
|
ENSP00000493657.1:n.-133G>A
|
|
ENST00000646777.1:n.773G>A
|
|
|
ENST00000647016.1:n.1077G>A
|
|
|
ENST00000647152.1:c.-133G>A
|
ENSP00000495893.1:n.-133G>A
|
|
ENST00000647209.1:c.*466G>A
|
ENSP00000495558.1:n.*466G>A
|
|
ENST00000647346.1:n.1617G>A
|
|
|
ENST00000299427.10:c.597G>A
|
ENSP00000299427.6:p.Gly199=
|
|
ENST00000428886.6:n.766G>A
|
|
|
ENST00000436873.6:c.450+294G>A
|
ENSP00000398136.2:n.450+294G>A
|
|
ENST00000524788.1:n.297G>A
|
|
|
ENST00000528571.5:c.*337G>A
|
ENSP00000434647.1:n.*337G>A
|
|
ENST00000528807.1:n.147G>A
|
|
|
ENST00000533371.5:c.-133G>A
|
ENSP00000437066.1:n.-133G>A
|
|
ENST00000534644.5:n.582G>A
|
|
|
ENST00000611494.4:c.597G>A
|
ENSP00000484546.1:p.Gly199=
|
|
NM_000391.3:c.597G>A
|
NP_000382.3:p.Gly199=
|
|
NM_000391.4:c.597G>A
MANE Select
|
NP_000382.3:p.Gly199=
|
|