ENST00000261304.7:c.581G=
MANE Select
|
ENSP00000261304.2:p.Gly194=
|
|
ENST00000261304.6:c.581G=
|
ENSP00000261304.2:p.Gly194=
|
|
ENST00000393568.8:c.512G=
|
ENSP00000377198.4:p.Gly171=
|
|
ENST00000393569.6:c.503G=
|
ENSP00000377199.2:p.Gly168=
|
|
ENST00000474294.6:n.571G=
|
|
|
ENST00000544807.6:c.413G=
|
ENSP00000437513.2:p.Gly138=
|
|
ENST00000554372.5:c.*330G=
|
ENSP00000451884.1:n.*330G=
|
|
ENST00000554916.5:n.460G=
|
|
|
ENST00000556261.5:n.282G=
|
|
|
ENST00000557316.5:c.581G=
|
ENSP00000452314.1:p.Gly194=
|
|
ENST00000622264.4:c.571G=
|
|
|
NM_000153.3:c.581G=
|
NP_000144.2:p.Gly194=
|
|
NM_001201401.1:c.512G=
|
NP_001188330.1:p.Gly171=
|
|
NM_001201402.1:c.503G=
|
NP_001188331.1:p.Gly168=
|
|
XM_011536618.1:c.413G=
|
XP_011534920.1:p.Gly138=
|
|
XM_011536618.2:c.413G=
|
XP_011534920.1:p.Gly138=
|
|
NM_000153.4:c.581G=
MANE Select
|
NP_000144.2:p.Gly194=
|
|
NM_001201401.2:c.512G=
|
NP_001188330.1:p.Gly171=
|
|
NM_001201402.2:c.503G=
|
NP_001188331.1:p.Gly168=
|
|