ENST00000682424.1:c.541G>T
|
ENSP00000507321.1:p.Gly181Cys
|
|
ENST00000299427.12:c.655G>T
MANE Select
|
ENSP00000299427.6:p.Gly219Cys
|
|
ENST00000436873.7:c.312+294G>T
|
|
|
ENST00000524788.2:n.1814G>T
|
|
|
ENST00000524903.2:n.1930G>T
|
|
|
ENST00000528807.2:n.311G>T
|
|
|
ENST00000530040.2:n.479+352G>T
|
|
|
ENST00000533371.6:c.-75G>T
|
ENSP00000437066.1:n.-75G>T
|
|
ENST00000534644.6:n.603G>T
|
|
|
ENST00000642892.1:c.-75G>T
|
ENSP00000494165.1:n.-75G>T
|
|
ENST00000643439.1:c.*395G>T
|
ENSP00000495849.1:n.*395G>T
|
|
ENST00000643479.1:n.684G>T
|
|
|
ENST00000643516.1:c.395+294G>T
|
|
|
ENST00000644151.1:n.2094G>T
|
|
|
ENST00000644218.1:c.655G>T
|
ENSP00000493574.1:p.Gly219Cys
|
|
ENST00000644683.1:c.*108G>T
|
ENSP00000494085.1:n.*108G>T
|
|
ENST00000644810.1:c.376G>T
|
ENSP00000495895.1:p.Gly126Cys
|
|
ENST00000644831.1:n.831G>T
|
|
|
ENST00000644933.1:c.-75G>T
|
ENSP00000496133.1:n.-75G>T
|
|
ENST00000645020.1:n.1830G>T
|
|
|
ENST00000645285.1:c.-75G>T
|
ENSP00000495058.1:n.-75G>T
|
|
ENST00000645331.1:n.1021G>T
|
|
|
ENST00000645620.1:c.-75G>T
|
ENSP00000493657.1:n.-75G>T
|
|
ENST00000646777.1:n.831G>T
|
|
|
ENST00000647016.1:n.1135G>T
|
|
|
ENST00000647152.1:c.-75G>T
|
ENSP00000495893.1:n.-75G>T
|
|
ENST00000647209.1:c.*524G>T
|
ENSP00000495558.1:n.*524G>T
|
|
ENST00000647346.1:n.1675G>T
|
|
|
ENST00000299427.10:c.655G>T
|
ENSP00000299427.6:p.Gly219Cys
|
|
ENST00000428886.6:n.824G>T
|
|
|
ENST00000436873.6:c.450+352G>T
|
ENSP00000398136.2:n.450+352G>T
|
|
ENST00000524788.1:n.355G>T
|
|
|
ENST00000528571.5:c.*395G>T
|
ENSP00000434647.1:n.*395G>T
|
|
ENST00000528807.1:n.205G>T
|
|
|
ENST00000533371.5:c.-75G>T
|
ENSP00000437066.1:n.-75G>T
|
|
ENST00000611494.4:c.655G>T
|
ENSP00000484546.1:p.Gly219Cys
|
|
NM_000391.3:c.655G>T
|
NP_000382.3:p.Gly219Cys
|
|
NM_000391.4:c.655G>T
MANE Select
|
NP_000382.3:p.Gly219Cys
|
|