ENST00000270357.10:c.1602G>T
MANE Select
|
ENSP00000270357.4:p.Glu534Asp
|
|
ENST00000270357.8:c.909G>T
|
ENSP00000270357.3:p.Glu303Asp
|
|
ENST00000437406.1:c.168G>T
|
ENSP00000403319.1:p.Glu56Asp
|
|
ENST00000451363.5:c.243G>T
|
ENSP00000414661.1:p.Glu81Asp
|
|
ENST00000464550.5:n.438G>T
|
|
|
ENST00000471657.1:n.405G>T
|
|
|
ENST00000481757.5:n.2536G>T
|
|
|
ENST00000486058.5:n.1715G>T
|
|
|
ENST00000493398.5:n.748G>T
|
|
|
NM_018226.4:c.1602G>T
|
NP_060696.4:p.Glu534Asp
|
|
XM_005247036.3:c.1569G>T
|
XP_005247093.1:p.Glu523Asp
|
|
NM_018226.5:c.1602G>T
|
NP_060696.4:p.Glu534Asp
|
|
XM_005247036.4:c.1569G>T
|
XP_005247093.1:p.Glu523Asp
|
|
NM_018226.6:c.1602G>T
MANE Select
|
NP_060696.4:p.Glu534Asp
|
|