|
NM_000153.4:c.121G=
MANE Select
|
NP_000144.2:p.Gly41=
|
|
ENST00000261304.7:c.121G=
MANE Select
|
ENSP00000261304.2:p.Gly41=
|
|
NM_000153.3:c.121G=
|
NP_000144.2:p.Gly41=
|
|
NM_001201401.1:c.121G=
|
NP_001188330.1:p.Gly41=
|
|
NM_001201401.2:c.121G=
|
NP_001188330.1:p.Gly41=
|
|
NM_001201402.1:c.117+339G=
|
NP_001188331.1:n.117+339G=
|
|
NM_001201402.2:c.117+339G=
|
NP_001188331.1:n.117+339G=
|
|
ENST00000261304.6:c.121G=
|
ENSP00000261304.2:p.Gly41=
|
|
ENST00000393568.8:c.121G=
|
ENSP00000377198.4:p.Gly41=
|
|
ENST00000393569.6:c.117+339G=
|
ENSP00000377199.2:n.117+339G=
|
|
ENST00000474294.6:n.111G=
|
|
|
ENST00000554372.5:c.121G=
|
ENSP00000451884.1:p.Gly41=
|
|
ENST00000556879.5:c.79G=
|
ENSP00000452208.1:p.Gly27=
|
|
ENST00000557316.5:c.121G=
|
ENSP00000452314.1:p.Gly41=
|
|
ENST00000622264.4:c.111G=
|
|