|
NM_002758.4:c.174A>T
MANE Select
|
NP_002749.2:p.Glu58Asp
|
|
ENST00000590474.7:c.174A>T
MANE Select
|
ENSP00000468348.1:p.Glu58Asp
|
|
NM_001330450.1:c.6A>T
|
NP_001317379.1:p.Glu2Asp
|
|
NM_001330450.2:c.6A>T
|
NP_001317379.1:p.Glu2Asp
|
|
NM_002758.3:c.174A>T
|
NP_002749.2:p.Glu58Asp
|
|
ENST00000359094.7:c.174A>T
|
ENSP00000351997.3:p.Glu58Asp
|
|
ENST00000586641.5:n.448A>T
|
|
|
ENST00000588110.5:c.183A>T
|
ENSP00000464916.1:p.Glu61Asp
|
|
ENST00000589295.5:c.6A>T
|
ENSP00000466143.1:p.Glu2Asp
|
|
ENST00000589647.5:c.6A>T
|
ENSP00000467213.1:p.Glu2Asp
|
|
ENST00000590474.5:c.174A>T
|
ENSP00000468348.1:p.Glu58Asp
|
|
ENST00000591445.1:n.490A>T
|
|
|
ENST00000613873.4:c.6A>T
|
ENSP00000477701.1:p.Glu2Asp
|
|
XM_005257515.1:c.6A>T
|
XP_005257572.1:p.Glu2Asp
|
|
XM_005257516.1:c.6A>T
|
XP_005257573.1:p.Glu2Asp
|
|
XM_005257516.2:c.6A>T
|
XP_005257573.1:p.Glu2Asp
|
|
XM_006721975.2:c.6A>T
|
XP_006722038.1:p.Glu2Asp
|
|
XM_006721975.3:c.6A>T
|
XP_006722038.1:p.Glu2Asp
|
|
XM_011525025.1:c.207A>T
|
XP_011523327.1:p.Glu69Asp
|
|
XM_011525026.1:c.183A>T
|
XP_011523328.1:p.Glu61Asp
|
|
XM_011525026.2:c.183A>T
|
XP_011523328.1:p.Glu61Asp
|
|
XM_011525027.1:c.6A>T
|
XP_011523329.1:p.Glu2Asp
|
|
XM_011525027.3:c.6A>T
|
XP_011523329.1:p.Glu2Asp
|