ENST00000394867.9:n.1567A>T
|
|
|
ENST00000688002.1:n.3279A>T
|
|
|
ENST00000688751.1:n.264A>T
|
|
|
ENST00000689792.1:n.1032A>T
|
|
|
ENST00000262948.10:c.1128A>T
MANE Select
|
ENSP00000262948.4:p.Glu376Asp
|
|
ENST00000262948.9:c.1128A>T
|
ENSP00000262948.3:p.Glu376Asp
|
|
ENST00000394867.8:c.837A>T
|
ENSP00000378336.1:p.Glu279Asp
|
|
ENST00000597263.5:n.313A>T
|
|
|
ENST00000599021.1:c.238A>T
|
|
|
ENST00000600584.5:n.2577A>T
|
|
|
ENST00000601786.5:n.1429A>T
|
|
|
NM_030662.3:c.1128A>T , LRG_750t1:c.1128A>T
|
NP_109587.1:p.Glu376Asp
|
|
XM_006722799.2:c.849A>T
|
XP_006722862.1:p.Glu283Asp
|
|
XM_011528133.1:c.558A>T
|
XP_011526435.1:p.Glu186Asp
|
|
NM_030662.4:c.1128A>T
MANE Select
|
NP_109587.1:p.Glu376Asp
|
|