ENST00000236671.7:c.1107C>T
MANE Select
|
ENSP00000236671.2:p.Gly369=
|
|
ENST00000367196.4:c.1002C>T
|
ENSP00000356164.4:p.Gly334=
|
|
ENST00000427721.3:c.532C>T
|
|
|
ENST00000429746.2:c.1002C>T
|
ENSP00000402586.2:p.Gly334=
|
|
ENST00000433655.6:c.*273C>T
|
ENSP00000404902.1:n.*273C>T
|
|
ENST00000438213.6:c.1224C>T
|
ENSP00000415036.2:p.Gly408=
|
|
ENST00000636397.1:c.1071+168C>T
|
ENSP00000489910.1:n.1071+168C>T
|
|
ENST00000636571.1:c.1086C>T
|
ENSP00000490770.1:p.Gly362=
|
|
ENST00000636579.1:c.72+168C>T
|
ENSP00000490489.1:n.72+168C>T
|
|
ENST00000636615.1:c.1071+168C>T
|
ENSP00000490014.1:n.1071+168C>T
|
|
ENST00000636843.1:c.1101C>T
|
ENSP00000490897.1:p.Gly367=
|
|
ENST00000637158.1:n.705C>T
|
|
|
ENST00000637381.2:n.3535C>T
|
|
|
ENST00000637387.1:c.1086C>T
|
ENSP00000490598.1:p.Gly362=
|
|
ENST00000637815.2:c.1089C>T
|
ENSP00000490344.1:p.Gly363=
|
|
ENST00000637915.1:c.1098C>T
|
ENSP00000490471.1:p.Gly366=
|
|
ENST00000637937.1:n.415C>T
|
|
|
ENST00000678991.1:c.*968C>T
|
ENSP00000503019.1:n.*968C>T
|
|
ENST00000236671.6:c.1107C>T
|
ENSP00000236671.2:p.Gly369=
|
|
ENST00000427721.2:c.471+168C>T
|
ENSP00000415840.2:n.471+168C>T
|
|
ENST00000429746.1:c.438C>T
|
ENSP00000402586.1:p.Gly146=
|
|
ENST00000433655.5:c.*273C>T
|
ENSP00000404902.1:n.*273C>T
|
|
NM_001909.4:c.1107C>T
|
NP_001900.1:p.Gly369=
|
|
NM_001909.5:c.1107C>T
MANE Select
|
NP_001900.1:p.Gly369=
|
|