ENST00000682424.1:c.631G>T
|
ENSP00000507321.1:p.Gly211Cys
|
|
ENST00000299427.12:c.745G>T
MANE Select
|
ENSP00000299427.6:p.Gly249Cys
|
|
ENST00000436873.7:c.312+499G>T
|
|
|
ENST00000524788.2:n.1904G>T
|
|
|
ENST00000524903.2:n.2020G>T
|
|
|
ENST00000528807.2:n.401G>T
|
|
|
ENST00000530040.2:n.480-299G>T
|
|
|
ENST00000533371.6:c.16G>T
|
ENSP00000437066.1:p.Gly6Cys
|
|
ENST00000642892.1:c.16G>T
|
ENSP00000494165.1:p.Gly6Cys
|
|
ENST00000643439.1:c.*485G>T
|
ENSP00000495849.1:n.*485G>T
|
|
ENST00000643479.1:n.774G>T
|
|
|
ENST00000643516.1:c.396-299G>T
|
|
|
ENST00000644151.1:n.2184G>T
|
|
|
ENST00000644218.1:c.745G>T
|
ENSP00000493574.1:p.Gly249Cys
|
|
ENST00000644683.1:c.*198G>T
|
ENSP00000494085.1:n.*198G>T
|
|
ENST00000644810.1:c.466G>T
|
ENSP00000495895.1:p.Gly156Cys
|
|
ENST00000644831.1:n.921G>T
|
|
|
ENST00000644933.1:c.16G>T
|
ENSP00000496133.1:p.Gly6Cys
|
|
ENST00000645020.1:n.2035G>T
|
|
|
ENST00000645285.1:c.16G>T
|
ENSP00000495058.1:p.Gly6Cys
|
|
ENST00000645331.1:n.1111G>T
|
|
|
ENST00000645620.1:c.16G>T
|
ENSP00000493657.1:p.Gly6Cys
|
|
ENST00000646777.1:n.921G>T
|
|
|
ENST00000647016.1:n.1225G>T
|
|
|
ENST00000647152.1:c.16G>T
|
ENSP00000495893.1:p.Gly6Cys
|
|
ENST00000647209.1:c.*614G>T
|
ENSP00000495558.1:n.*614G>T
|
|
ENST00000647346.1:n.1765G>T
|
|
|
ENST00000299427.10:c.745G>T
|
ENSP00000299427.6:p.Gly249Cys
|
|
ENST00000436873.6:c.451-299G>T
|
ENSP00000398136.2:n.451-299G>T
|
|
ENST00000524788.1:n.445G>T
|
|
|
ENST00000528807.1:n.295G>T
|
|
|
ENST00000533371.5:c.16G>T
|
ENSP00000437066.1:p.Gly6Cys
|
|
ENST00000611494.4:c.745G>T
|
ENSP00000484546.1:p.Gly249Cys
|
|
NM_000391.3:c.745G>T
|
NP_000382.3:p.Gly249Cys
|
|
NM_000391.4:c.745G>T
MANE Select
|
NP_000382.3:p.Gly249Cys
|
|