ENST00000236671.7:c.946G>T
MANE Select
|
ENSP00000236671.2:p.Gly316Trp
|
|
ENST00000367196.4:c.841G>T
|
ENSP00000356164.4:p.Gly281Trp
|
|
ENST00000427721.3:c.371G>T
|
|
|
ENST00000429746.2:c.841G>T
|
ENSP00000402586.2:p.Gly281Trp
|
|
ENST00000433655.6:c.*112G>T
|
ENSP00000404902.1:n.*112G>T
|
|
ENST00000438213.6:c.1063G>T
|
ENSP00000415036.2:p.Gly355Trp
|
|
ENST00000497544.3:n.562G>T
|
|
|
ENST00000636397.1:c.946G>T
|
ENSP00000489910.1:p.Gly316Trp
|
|
ENST00000636571.1:c.925G>T
|
ENSP00000490770.1:p.Gly309Trp
|
|
ENST00000636615.1:c.946G>T
|
ENSP00000490014.1:p.Gly316Trp
|
|
ENST00000636843.1:c.940G>T
|
ENSP00000490897.1:p.Gly314Trp
|
|
ENST00000637158.1:n.544G>T
|
|
|
ENST00000637381.2:n.3374G>T
|
|
|
ENST00000637387.1:c.946G>T
|
ENSP00000490598.1:p.Gly316Trp
|
|
ENST00000637815.2:c.928G>T
|
ENSP00000490344.1:p.Gly310Trp
|
|
ENST00000637915.1:c.946G>T
|
ENSP00000490471.1:p.Gly316Trp
|
|
ENST00000637937.1:n.254G>T
|
|
|
ENST00000678991.1:c.*807G>T
|
ENSP00000503019.1:n.*807G>T
|
|
ENST00000236671.6:c.946G>T
|
ENSP00000236671.2:p.Gly316Trp
|
|
ENST00000427721.2:c.346G>T
|
ENSP00000415840.2:p.Gly116Trp
|
|
ENST00000429746.1:c.277G>T
|
ENSP00000402586.1:p.Gly93Trp
|
|
ENST00000433655.5:c.*112G>T
|
ENSP00000404902.1:n.*112G>T
|
|
ENST00000497544.1:n.562G>T
|
|
|
NM_001909.4:c.946G>T
|
NP_001900.1:p.Gly316Trp
|
|
NM_001909.5:c.946G>T
MANE Select
|
NP_001900.1:p.Gly316Trp
|
|