ENST00000563193.2:c.846G>T
|
ENSP00000455533.2:p.Glu282Asp
|
|
ENST00000697561.1:c.*275G>T
|
ENSP00000513337.1:n.*275G>T
|
|
ENST00000697562.1:c.846G>T
|
ENSP00000513338.1:p.Glu282Asp
|
|
ENST00000697563.1:c.*692G>T
|
ENSP00000513339.1:n.*692G>T
|
|
ENST00000697564.1:c.729G>T
|
ENSP00000513340.1:p.Glu243Asp
|
|
ENST00000697565.1:n.786G>T
|
|
|
ENST00000697581.1:c.*840G>T
|
ENSP00000513346.1:n.*840G>T
|
|
ENST00000697582.1:c.846G>T
|
ENSP00000513347.1:p.Glu282Asp
|
|
ENST00000697583.1:c.645G>T
|
ENSP00000513349.1:p.Glu215Asp
|
|
ENST00000697584.1:c.645G>T
|
ENSP00000513350.1:p.Glu215Asp
|
|
ENST00000697585.1:c.645G>T
|
ENSP00000513351.1:p.Glu215Asp
|
|
ENST00000697586.1:c.645G>T
|
ENSP00000513352.1:p.Glu215Asp
|
|
ENST00000697587.1:c.645G>T
|
ENSP00000513353.1:p.Glu215Asp
|
|
ENST00000564138.6:c.846G>T
MANE Select
|
ENSP00000482457.1:p.Glu282Asp
|
|
ENST00000359376.7:c.846G>T
|
ENSP00000352336.4:p.Glu282Asp
|
|
ENST00000563193.1:c.154G>T
|
|
|
ENST00000564138.5:c.846G>T
|
ENSP00000482457.1:p.Glu282Asp
|
|
ENST00000567980.5:n.1090G>T
|
|
|
NM_002661.4:c.846G>T
|
NP_002652.2:p.Glu282Asp
|
|
XM_011523108.1:c.960G>T
|
XP_011521410.1:p.Glu320Asp
|
|
NM_002661.5:c.846G>T
MANE Select
|
NP_002652.2:p.Glu282Asp
|
|