ENST00000456935.7:c.538G=
MANE Select
|
ENSP00000395473.2:p.Glu180=
|
|
ENST00000221363.8:c.538G=
|
ENSP00000221363.4:p.Glu180=
|
|
ENST00000456935.6:c.538G=
|
ENSP00000395473.2:p.Glu180=
|
|
ENST00000466794.5:n.520G=
|
|
|
ENST00000486847.2:c.333+468G=
|
ENSP00000470174.1:n.333+468G=
|
|
ENST00000596512.5:n.476G=
|
|
|
ENST00000597961.1:c.529G=
|
ENSP00000472710.1:p.Glu177=
|
|
NM_000528.3:c.538G=
|
NP_000519.2:p.Glu180=
|
|
NM_001173498.1:c.538G=
|
NP_001166969.1:p.Glu180=
|
|
XM_005259913.1:c.538G=
|
XP_005259970.1:p.Glu180=
|
|
XM_005259913.2:c.538G=
|
XP_005259970.1:p.Glu180=
|
|
XM_024451518.1:c.-481G=
|
XP_024307286.1:n.-481G=
|
|
NM_000528.4:c.538G=
MANE Select
|
NP_000519.2:p.Glu180=
|
|
NM_001173498.2:c.538G=
|
NP_001166969.1:p.Glu180=
|
|