ENST00000682424.1:c.399G=
|
ENSP00000507321.1:p.Gly133=
|
|
ENST00000299427.12:c.513G=
MANE Select
|
ENSP00000299427.6:p.Gly171=
|
|
ENST00000428886.7:n.748G=
|
|
|
ENST00000436873.7:c.312+152G=
|
|
|
ENST00000524788.2:n.1672G=
|
|
|
ENST00000524903.2:n.1788G=
|
|
|
ENST00000528807.2:n.169G=
|
|
|
ENST00000530040.2:n.479+210G=
|
|
|
ENST00000533371.6:c.-217G=
|
ENSP00000437066.1:n.-217G=
|
|
ENST00000534644.6:n.461G=
|
|
|
ENST00000642892.1:c.-217G=
|
ENSP00000494165.1:n.-217G=
|
|
ENST00000643439.1:c.*253G=
|
ENSP00000495849.1:n.*253G=
|
|
ENST00000643479.1:n.542G=
|
|
|
ENST00000643516.1:c.395+152G=
|
|
|
ENST00000644151.1:n.1952G=
|
|
|
ENST00000644218.1:c.513G=
|
ENSP00000493574.1:p.Gly171=
|
|
ENST00000644683.1:c.455G=
|
ENSP00000494085.1:p.Gly152=
|
|
ENST00000644810.1:c.234G=
|
ENSP00000495895.1:p.Gly78=
|
|
ENST00000644831.1:n.689G=
|
|
|
ENST00000644933.1:c.-217G=
|
ENSP00000496133.1:n.-217G=
|
|
ENST00000645020.1:n.1688G=
|
|
|
ENST00000645285.1:c.-217G=
|
ENSP00000495058.1:n.-217G=
|
|
ENST00000645331.1:n.879G=
|
|
|
ENST00000645620.1:c.-217G=
|
ENSP00000493657.1:n.-217G=
|
|
ENST00000646777.1:n.689G=
|
|
|
ENST00000647016.1:n.993G=
|
|
|
ENST00000647152.1:c.-217G=
|
ENSP00000495893.1:n.-217G=
|
|
ENST00000647209.1:c.*382G=
|
ENSP00000495558.1:n.*382G=
|
|
ENST00000647346.1:n.1533G=
|
|
|
ENST00000299427.10:c.513G=
|
ENSP00000299427.6:p.Gly171=
|
|
ENST00000428886.6:n.682G=
|
|
|
ENST00000436873.6:c.450+210G=
|
ENSP00000398136.2:n.450+210G=
|
|
ENST00000524788.1:n.213G=
|
|
|
ENST00000528571.5:c.*253G=
|
ENSP00000434647.1:n.*253G=
|
|
ENST00000528807.1:n.63G=
|
|
|
ENST00000533371.5:c.-217G=
|
ENSP00000437066.1:n.-217G=
|
|
ENST00000534644.5:n.498G=
|
|
|
ENST00000611494.4:c.513G=
|
ENSP00000484546.1:p.Gly171=
|
|
NM_000391.3:c.513G=
|
NP_000382.3:p.Gly171=
|
|
NM_000391.4:c.513G=
MANE Select
|
NP_000382.3:p.Gly171=
|
|