|
ENST00000682424.1:c.192G>T
|
ENSP00000507321.1:p.Trp64Cys
|
|
|
ENST00000299427.12:c.306G>T
MANE Select
|
ENSP00000299427.6:p.Trp102Cys
|
|
|
ENST00000428886.7:n.394G>T
|
|
|
|
ENST00000436873.7:c.110G>T
|
|
|
|
ENST00000524788.2:n.1318G>T
|
|
|
|
ENST00000524903.2:n.1434G>T
|
|
|
|
ENST00000528571.6:c.*46G>T
|
ENSP00000434647.1:n.*46G>T
|
|
|
ENST00000530040.2:n.335G>T
|
|
|
|
ENST00000533371.6:c.-424G>T
|
ENSP00000437066.1:n.-424G>T
|
|
|
ENST00000534644.6:n.307G>T
|
|
|
|
ENST00000642892.1:c.-371G>T
|
ENSP00000494165.1:n.-371G>T
|
|
|
ENST00000643439.1:c.*46G>T
|
ENSP00000495849.1:n.*46G>T
|
|
|
ENST00000643479.1:n.335G>T
|
|
|
|
ENST00000643516.1:c.193G>T
|
|
|
|
ENST00000644151.1:n.1598G>T
|
|
|
|
ENST00000644218.1:c.306G>T
|
ENSP00000493574.1:p.Trp102Cys
|
|
|
ENST00000644683.1:c.306G>T
|
ENSP00000494085.1:p.Trp102Cys
|
|
|
ENST00000644810.1:c.230-547G>T
|
ENSP00000495895.1:n.230-547G>T
|
|
|
ENST00000644831.1:n.335G>T
|
|
|
|
ENST00000644933.1:c.-424G>T
|
ENSP00000496133.1:n.-424G>T
|
|
|
ENST00000645020.1:n.1334G>T
|
|
|
|
ENST00000645285.1:c.-424G>T
|
ENSP00000495058.1:n.-424G>T
|
|
|
ENST00000645331.1:n.328G>T
|
|
|
|
ENST00000645620.1:c.-366G>T
|
ENSP00000493657.1:n.-366G>T
|
|
|
ENST00000646777.1:n.335G>T
|
|
|
|
ENST00000647016.1:n.639G>T
|
|
|
|
ENST00000647152.1:c.-424G>T
|
ENSP00000495893.1:n.-424G>T
|
|
|
ENST00000647209.1:c.*175G>T
|
ENSP00000495558.1:n.*175G>T
|
|
|
ENST00000647346.1:n.1326G>T
|
|
|
|
ENST00000299427.10:c.306G>T
|
ENSP00000299427.6:p.Trp102Cys
|
|
|
ENST00000428886.6:n.328G>T
|
|
|
|
ENST00000436873.6:c.306G>T
|
ENSP00000398136.2:p.Trp102Cys
|
|
|
ENST00000528571.5:c.*46G>T
|
ENSP00000434647.1:n.*46G>T
|
|
|
ENST00000530040.1:n.418G>T
|
|
|
|
ENST00000533371.5:c.-424G>T
|
ENSP00000437066.1:n.-424G>T
|
|
|
ENST00000534644.5:n.291G>T
|
|
|
|
ENST00000611494.4:c.306G>T
|
ENSP00000484546.1:p.Trp102Cys
|
|
|
NM_000391.3:c.306G>T
|
NP_000382.3:p.Trp102Cys
|
|
|
NM_000391.4:c.306G>T
MANE Select
|
NP_000382.3:p.Trp102Cys
|
|
