ENST00000228284.8:c.1807G=
|
ENSP00000228284.4:p.Glu603=
|
|
ENST00000546815.6:c.1753G=
MANE Select
|
ENSP00000449386.2:p.Glu585=
|
|
ENST00000651280.1:c.*909G=
|
ENSP00000498612.1:n.*909G=
|
|
ENST00000228284.7:c.1753G=
|
ENSP00000228284.3:p.Glu585=
|
|
ENST00000431469.6:c.1645G=
|
ENSP00000414453.2:p.Glu549=
|
|
ENST00000546728.5:c.*647G=
|
ENSP00000449743.1:n.*647G=
|
|
ENST00000546815.5:c.1807G=
|
ENSP00000449386.1:p.Glu603=
|
|
ENST00000547528.5:c.*917G=
|
ENSP00000446577.1:n.*917G=
|
|
ENST00000548582.5:n.480G=
|
|
|
ENST00000619503.4:n.689G=
|
|
|
NM_014706.3:c.1753G=
|
NP_055521.1:p.Glu585=
|
|
XM_005269241.3:c.1807G=
|
XP_005269298.1:p.Glu603=
|
|
XM_011539026.1:c.889G=
|
XP_011537328.1:p.Glu297=
|
|
NM_014706.4:c.1753G=
MANE Select
|
NP_055521.1:p.Glu585=
|
|
XM_005269241.5:c.1807G=
|
XP_005269298.1:p.Glu603=
|
|
XM_024449284.1:c.889G=
|
XP_024305052.1:p.Glu297=
|
|