ENST00000682424.1:c.736G>T
|
ENSP00000507321.1:p.Gly246Cys
|
|
ENST00000299427.12:c.850G>T
MANE Select
|
ENSP00000299427.6:p.Gly284Cys
|
|
ENST00000436873.7:c.312+604G>T
|
|
|
ENST00000524788.2:n.2009G>T
|
|
|
ENST00000524903.2:n.2125G>T
|
|
|
ENST00000528807.2:n.506G>T
|
|
|
ENST00000530040.2:n.480-194G>T
|
|
|
ENST00000533371.6:c.121G>T
|
ENSP00000437066.1:p.Gly41Cys
|
|
ENST00000642892.1:c.121G>T
|
ENSP00000494165.1:p.Gly41Cys
|
|
ENST00000643439.1:c.*590G>T
|
ENSP00000495849.1:n.*590G>T
|
|
ENST00000643479.1:n.879G>T
|
|
|
ENST00000643516.1:c.396-194G>T
|
|
|
ENST00000644151.1:n.2289G>T
|
|
|
ENST00000644218.1:c.850G>T
|
ENSP00000493574.1:p.Gly284Cys
|
|
ENST00000644683.1:c.*303G>T
|
ENSP00000494085.1:n.*303G>T
|
|
ENST00000644810.1:c.571G>T
|
ENSP00000495895.1:p.Gly191Cys
|
|
ENST00000644831.1:n.1026G>T
|
|
|
ENST00000644933.1:c.121G>T
|
ENSP00000496133.1:p.Gly41Cys
|
|
ENST00000645020.1:n.2140G>T
|
|
|
ENST00000645285.1:c.121G>T
|
ENSP00000495058.1:p.Gly41Cys
|
|
ENST00000645331.1:n.1216G>T
|
|
|
ENST00000645620.1:c.121G>T
|
ENSP00000493657.1:p.Gly41Cys
|
|
ENST00000646777.1:n.1026G>T
|
|
|
ENST00000647016.1:n.1330G>T
|
|
|
ENST00000647152.1:c.121G>T
|
ENSP00000495893.1:p.Gly41Cys
|
|
ENST00000647209.1:c.*719G>T
|
ENSP00000495558.1:n.*719G>T
|
|
ENST00000647346.1:n.1870G>T
|
|
|
ENST00000299427.10:c.850G>T
|
ENSP00000299427.6:p.Gly284Cys
|
|
ENST00000436873.6:c.451-194G>T
|
ENSP00000398136.2:n.451-194G>T
|
|
ENST00000524788.1:n.550G>T
|
|
|
ENST00000528807.1:n.400G>T
|
|
|
ENST00000533371.5:c.121G>T
|
ENSP00000437066.1:p.Gly41Cys
|
|
ENST00000611494.4:c.850G>T
|
ENSP00000484546.1:p.Gly284Cys
|
|
NM_000391.3:c.850G>T
|
NP_000382.3:p.Gly284Cys
|
|
NM_000391.4:c.850G>T
MANE Select
|
NP_000382.3:p.Gly284Cys
|
|