ENST00000563193.2:c.768G>A
|
ENSP00000455533.2:p.Glu256=
|
|
ENST00000697561.1:c.*197G>A
|
ENSP00000513337.1:n.*197G>A
|
|
ENST00000697562.1:c.768G>A
|
ENSP00000513338.1:p.Glu256=
|
|
ENST00000697563.1:c.*614G>A
|
ENSP00000513339.1:n.*614G>A
|
|
ENST00000697564.1:c.651G>A
|
ENSP00000513340.1:p.Glu217=
|
|
ENST00000697565.1:n.708G>A
|
|
|
ENST00000697581.1:c.*762G>A
|
ENSP00000513346.1:n.*762G>A
|
|
ENST00000697582.1:c.768G>A
|
ENSP00000513347.1:p.Glu256=
|
|
ENST00000697583.1:c.567G>A
|
ENSP00000513349.1:p.Glu189=
|
|
ENST00000697584.1:c.567G>A
|
ENSP00000513350.1:p.Glu189=
|
|
ENST00000697585.1:c.567G>A
|
ENSP00000513351.1:p.Glu189=
|
|
ENST00000697586.1:c.567G>A
|
ENSP00000513352.1:p.Glu189=
|
|
ENST00000697587.1:c.567G>A
|
ENSP00000513353.1:p.Glu189=
|
|
ENST00000564138.6:c.768G>A
MANE Select
|
ENSP00000482457.1:p.Glu256=
|
|
ENST00000359376.7:c.768G>A
|
ENSP00000352336.4:p.Glu256=
|
|
ENST00000563193.1:c.76G>A
|
|
|
ENST00000564138.5:c.768G>A
|
ENSP00000482457.1:p.Glu256=
|
|
ENST00000567980.5:n.1012G>A
|
|
|
NM_002661.4:c.768G>A
|
NP_002652.2:p.Glu256=
|
|
XM_011523108.1:c.882G>A
|
XP_011521410.1:p.Glu294=
|
|
NM_002661.5:c.768G>A
MANE Select
|
NP_002652.2:p.Glu256=
|
|