ENST00000682424.1:c.807G>T
|
ENSP00000507321.1:p.Trp269Cys
|
|
ENST00000299427.12:c.921G>T
MANE Select
|
ENSP00000299427.6:p.Trp307Cys
|
|
ENST00000436873.7:c.313-395G>T
|
|
|
ENST00000530040.2:n.514G>T
|
|
|
ENST00000533371.6:c.192G>T
|
ENSP00000437066.1:p.Trp64Cys
|
|
ENST00000642892.1:c.192G>T
|
ENSP00000494165.1:p.Trp64Cys
|
|
ENST00000643342.1:c.11G>T
|
|
|
ENST00000643439.1:c.*661G>T
|
ENSP00000495849.1:n.*661G>T
|
|
ENST00000643479.1:n.1107G>T
|
|
|
ENST00000643516.1:c.430G>T
|
|
|
ENST00000644218.1:c.886+192G>T
|
ENSP00000493574.1:n.886+192G>T
|
|
ENST00000644683.1:c.*374G>T
|
ENSP00000494085.1:n.*374G>T
|
|
ENST00000644810.1:c.642G>T
|
ENSP00000495895.1:p.Trp214Cys
|
|
ENST00000644831.1:n.1097G>T
|
|
|
ENST00000644933.1:c.192G>T
|
ENSP00000496133.1:p.Trp64Cys
|
|
ENST00000645285.1:c.157+192G>T
|
ENSP00000495058.1:n.157+192G>T
|
|
ENST00000645331.1:n.1444G>T
|
|
|
ENST00000645620.1:c.192G>T
|
ENSP00000493657.1:p.Trp64Cys
|
|
ENST00000646691.1:n.14G>T
|
|
|
ENST00000646777.1:n.1254G>T
|
|
|
ENST00000647016.1:n.1401G>T
|
|
|
ENST00000647152.1:c.192G>T
|
ENSP00000495893.1:p.Trp64Cys
|
|
ENST00000647209.1:c.*790G>T
|
ENSP00000495558.1:n.*790G>T
|
|
ENST00000647346.1:n.1941G>T
|
|
|
ENST00000299427.10:c.921G>T
|
ENSP00000299427.6:p.Trp307Cys
|
|
ENST00000436873.6:c.485G>T
|
ENSP00000398136.2:p.Gly162Val
|
|
ENST00000533371.5:c.192G>T
|
ENSP00000437066.1:p.Trp64Cys
|
|
ENST00000611494.4:c.921G>T
|
ENSP00000484546.1:p.Trp307Cys
|
|
NM_000391.3:c.921G>T
|
NP_000382.3:p.Trp307Cys
|
|
NM_000391.4:c.921G>T
MANE Select
|
NP_000382.3:p.Trp307Cys
|
|