ENST00000236671.7:c.1213G>T
MANE Select
|
ENSP00000236671.2:p.Gly405Cys
|
|
ENST00000367196.4:c.1108G>T
|
ENSP00000356164.4:p.Gly370Cys
|
|
ENST00000427721.3:c.634+4G>T
|
|
|
ENST00000429746.2:c.1108G>T
|
ENSP00000402586.2:p.Gly370Cys
|
|
ENST00000433655.6:c.*379G>T
|
ENSP00000404902.1:n.*379G>T
|
|
ENST00000438213.6:c.1330G>T
|
ENSP00000415036.2:p.Gly444Cys
|
|
ENST00000636397.1:c.1071+274G>T
|
ENSP00000489910.1:n.1071+274G>T
|
|
ENST00000636571.1:c.1192G>T
|
ENSP00000490770.1:p.Gly398Cys
|
|
ENST00000636579.1:c.72+274G>T
|
ENSP00000490489.1:n.72+274G>T
|
|
ENST00000636615.1:c.1071+274G>T
|
ENSP00000490014.1:n.1071+274G>T
|
|
ENST00000636843.1:c.1207G>T
|
ENSP00000490897.1:p.Gly403Cys
|
|
ENST00000637158.1:n.811G>T
|
|
|
ENST00000637381.2:n.3641G>T
|
|
|
ENST00000637387.1:c.1192G>T
|
ENSP00000490598.1:p.Gly398Cys
|
|
ENST00000637815.2:c.1195G>T
|
ENSP00000490344.1:p.Gly399Cys
|
|
ENST00000637915.1:c.1204G>T
|
ENSP00000490471.1:p.Gly402Cys
|
|
ENST00000637937.1:n.521G>T
|
|
|
ENST00000678991.1:c.*1074G>T
|
ENSP00000503019.1:n.*1074G>T
|
|
ENST00000236671.6:c.1213G>T
|
ENSP00000236671.2:p.Gly405Cys
|
|
ENST00000427721.2:c.471+274G>T
|
ENSP00000415840.2:n.471+274G>T
|
|
ENST00000429746.1:c.544G>T
|
ENSP00000402586.1:p.Gly182Cys
|
|
ENST00000433655.5:c.*379G>T
|
ENSP00000404902.1:n.*379G>T
|
|
NM_001909.4:c.1213G>T
|
NP_001900.1:p.Gly405Cys
|
|
NM_001909.5:c.1213G>T
MANE Select
|
NP_001900.1:p.Gly405Cys
|
|