ENST00000270357.10:c.1641G>A
MANE Select
|
ENSP00000270357.4:p.Gln547=
|
|
ENST00000270357.8:c.948G>A
|
ENSP00000270357.3:p.Gln316=
|
|
ENST00000437406.1:c.207G>A
|
ENSP00000403319.1:p.Gln69=
|
|
ENST00000451363.5:c.282G>A
|
ENSP00000414661.1:p.Gln94=
|
|
ENST00000464550.5:n.477G>A
|
|
|
ENST00000471657.1:n.444G>A
|
|
|
ENST00000481757.5:n.2575G>A
|
|
|
ENST00000486058.5:n.1754G>A
|
|
|
ENST00000493398.5:n.787G>A
|
|
|
NM_018226.4:c.1641G>A
|
NP_060696.4:p.Gln547=
|
|
XM_005247036.3:c.1608G>A
|
XP_005247093.1:p.Gln536=
|
|
NM_018226.5:c.1641G>A
|
NP_060696.4:p.Gln547=
|
|
XM_005247036.4:c.1608G>A
|
XP_005247093.1:p.Gln536=
|
|
NM_018226.6:c.1641G>A
MANE Select
|
NP_060696.4:p.Gln547=
|
|