ENST00000682424.1:c.1447G>T
|
ENSP00000507321.1:p.Gly483Cys
|
|
ENST00000299427.12:c.1561G>T
MANE Select
|
ENSP00000299427.6:p.Gly521Cys
|
|
ENST00000524611.2:n.600G>T
|
|
|
ENST00000524924.2:n.681G>T
|
|
|
ENST00000533371.6:c.832G>T
|
ENSP00000437066.1:p.Gly278Cys
|
|
ENST00000642892.1:c.832G>T
|
ENSP00000494165.1:p.Gly278Cys
|
|
ENST00000643342.1:c.634G>T
|
|
|
ENST00000643439.1:c.*1301G>T
|
ENSP00000495849.1:n.*1301G>T
|
|
ENST00000643479.1:n.1747G>T
|
|
|
ENST00000643516.1:c.1070G>T
|
|
|
ENST00000644218.1:c.1372G>T
|
ENSP00000493574.1:p.Gly458Cys
|
|
ENST00000644683.1:c.*1014G>T
|
ENSP00000494085.1:n.*1014G>T
|
|
ENST00000644810.1:c.1282G>T
|
ENSP00000495895.1:p.Gly428Cys
|
|
ENST00000644831.1:n.1737G>T
|
|
|
ENST00000644933.1:c.*427G>T
|
ENSP00000496133.1:n.*427G>T
|
|
ENST00000645285.1:c.*427G>T
|
ENSP00000495058.1:n.*427G>T
|
|
ENST00000645331.1:n.2766G>T
|
|
|
ENST00000645620.1:c.832G>T
|
ENSP00000493657.1:p.Gly278Cys
|
|
ENST00000646691.1:n.1448G>T
|
|
|
ENST00000646777.1:n.1894G>T
|
|
|
ENST00000647016.1:n.2041G>T
|
|
|
ENST00000647152.1:c.832G>T
|
ENSP00000495893.1:p.Gly278Cys
|
|
ENST00000647209.1:c.*1430G>T
|
ENSP00000495558.1:n.*1430G>T
|
|
ENST00000647346.1:n.2581G>T
|
|
|
ENST00000299427.10:c.1561G>T
|
ENSP00000299427.6:p.Gly521Cys
|
|
ENST00000524611.1:n.439G>T
|
|
|
ENST00000533371.5:c.832G>T
|
ENSP00000437066.1:p.Gly278Cys
|
|
ENST00000611494.4:c.1561G>T
|
ENSP00000484546.1:p.Gly521Cys
|
|
NM_000391.3:c.1561G>T
|
NP_000382.3:p.Gly521Cys
|
|
NM_000391.4:c.1561G>T
MANE Select
|
NP_000382.3:p.Gly521Cys
|
|