ENST00000682424.1:c.529G>T
|
ENSP00000507321.1:p.Asp177Tyr
|
|
ENST00000299427.12:c.643G>T
MANE Select
|
ENSP00000299427.6:p.Asp215Tyr
|
|
ENST00000436873.7:c.312+282G>T
|
|
|
ENST00000524788.2:n.1802G>T
|
|
|
ENST00000524903.2:n.1918G>T
|
|
|
ENST00000528807.2:n.299G>T
|
|
|
ENST00000530040.2:n.479+340G>T
|
|
|
ENST00000533371.6:c.-87G>T
|
ENSP00000437066.1:n.-87G>T
|
|
ENST00000534644.6:n.591G>T
|
|
|
ENST00000642892.1:c.-87G>T
|
ENSP00000494165.1:n.-87G>T
|
|
ENST00000643439.1:c.*383G>T
|
ENSP00000495849.1:n.*383G>T
|
|
ENST00000643479.1:n.672G>T
|
|
|
ENST00000643516.1:c.395+282G>T
|
|
|
ENST00000644151.1:n.2082G>T
|
|
|
ENST00000644218.1:c.643G>T
|
ENSP00000493574.1:p.Asp215Tyr
|
|
ENST00000644683.1:c.*96G>T
|
ENSP00000494085.1:n.*96G>T
|
|
ENST00000644810.1:c.364G>T
|
ENSP00000495895.1:p.Asp122Tyr
|
|
ENST00000644831.1:n.819G>T
|
|
|
ENST00000644933.1:c.-87G>T
|
ENSP00000496133.1:n.-87G>T
|
|
ENST00000645020.1:n.1818G>T
|
|
|
ENST00000645285.1:c.-87G>T
|
ENSP00000495058.1:n.-87G>T
|
|
ENST00000645331.1:n.1009G>T
|
|
|
ENST00000645620.1:c.-87G>T
|
ENSP00000493657.1:n.-87G>T
|
|
ENST00000646777.1:n.819G>T
|
|
|
ENST00000647016.1:n.1123G>T
|
|
|
ENST00000647152.1:c.-87G>T
|
ENSP00000495893.1:n.-87G>T
|
|
ENST00000647209.1:c.*512G>T
|
ENSP00000495558.1:n.*512G>T
|
|
ENST00000647346.1:n.1663G>T
|
|
|
ENST00000299427.10:c.643G>T
|
ENSP00000299427.6:p.Asp215Tyr
|
|
ENST00000428886.6:n.812G>T
|
|
|
ENST00000436873.6:c.450+340G>T
|
ENSP00000398136.2:n.450+340G>T
|
|
ENST00000524788.1:n.343G>T
|
|
|
ENST00000528571.5:c.*383G>T
|
ENSP00000434647.1:n.*383G>T
|
|
ENST00000528807.1:n.193G>T
|
|
|
ENST00000533371.5:c.-87G>T
|
ENSP00000437066.1:n.-87G>T
|
|
ENST00000534644.5:n.628G>T
|
|
|
ENST00000611494.4:c.643G>T
|
ENSP00000484546.1:p.Asp215Tyr
|
|
NM_000391.3:c.643G>T
|
NP_000382.3:p.Asp215Tyr
|
|
NM_000391.4:c.643G>T
MANE Select
|
NP_000382.3:p.Asp215Tyr
|
|