|
ENST00000682424.1:c.237G>T
|
ENSP00000507321.1:p.Gln79His
|
|
|
ENST00000299427.12:c.351G>T
MANE Select
|
ENSP00000299427.6:p.Gln117His
|
|
|
ENST00000428886.7:n.439G>T
|
|
|
|
ENST00000436873.7:c.155G>T
|
|
|
|
ENST00000524788.2:n.1363G>T
|
|
|
|
ENST00000524903.2:n.1479G>T
|
|
|
|
ENST00000528571.6:c.*91G>T
|
ENSP00000434647.1:n.*91G>T
|
|
|
ENST00000530040.2:n.380G>T
|
|
|
|
ENST00000533371.6:c.-379G>T
|
ENSP00000437066.1:n.-379G>T
|
|
|
ENST00000534644.6:n.352G>T
|
|
|
|
ENST00000642892.1:c.-326G>T
|
ENSP00000494165.1:n.-326G>T
|
|
|
ENST00000643439.1:c.*91G>T
|
ENSP00000495849.1:n.*91G>T
|
|
|
ENST00000643479.1:n.380G>T
|
|
|
|
ENST00000643516.1:c.238G>T
|
|
|
|
ENST00000644151.1:n.1643G>T
|
|
|
|
ENST00000644218.1:c.351G>T
|
ENSP00000493574.1:p.Gln117His
|
|
|
ENST00000644683.1:c.351G>T
|
ENSP00000494085.1:p.Gln117His
|
|
|
ENST00000644810.1:c.230-502G>T
|
ENSP00000495895.1:n.230-502G>T
|
|
|
ENST00000644831.1:n.380G>T
|
|
|
|
ENST00000644933.1:c.-379G>T
|
ENSP00000496133.1:n.-379G>T
|
|
|
ENST00000645020.1:n.1379G>T
|
|
|
|
ENST00000645285.1:c.-379G>T
|
ENSP00000495058.1:n.-379G>T
|
|
|
ENST00000645331.1:n.373G>T
|
|
|
|
ENST00000645620.1:c.-321G>T
|
ENSP00000493657.1:n.-321G>T
|
|
|
ENST00000646777.1:n.380G>T
|
|
|
|
ENST00000647016.1:n.684G>T
|
|
|
|
ENST00000647152.1:c.-379G>T
|
ENSP00000495893.1:n.-379G>T
|
|
|
ENST00000647209.1:c.*220G>T
|
ENSP00000495558.1:n.*220G>T
|
|
|
ENST00000647346.1:n.1371G>T
|
|
|
|
ENST00000299427.10:c.351G>T
|
ENSP00000299427.6:p.Gln117His
|
|
|
ENST00000428886.6:n.373G>T
|
|
|
|
ENST00000436873.6:c.351G>T
|
ENSP00000398136.2:p.Gln117His
|
|
|
ENST00000528571.5:c.*91G>T
|
ENSP00000434647.1:n.*91G>T
|
|
|
ENST00000530040.1:n.463G>T
|
|
|
|
ENST00000533371.5:c.-379G>T
|
ENSP00000437066.1:n.-379G>T
|
|
|
ENST00000534644.5:n.336G>T
|
|
|
|
ENST00000611494.4:c.351G>T
|
ENSP00000484546.1:p.Gln117His
|
|
|
NM_000391.3:c.351G>T
|
NP_000382.3:p.Gln117His
|
|
|
NM_000391.4:c.351G>T
MANE Select
|
NP_000382.3:p.Gln117His
|
|
