|
NM_015629.4:c.429C>T
MANE Select
|
NP_056444.3:p.Gly143=
|
|
ENST00000321030.9:c.429C>T
MANE Select
|
ENSP00000324122.4:p.Gly143=
|
|
NM_015629.3:c.429C>T
|
NP_056444.3:p.Gly143=
|
|
ENST00000321030.8:c.429C>T
|
ENSP00000324122.4:p.Gly143=
|
|
ENST00000391755.1:c.429C>T
|
ENSP00000375635.1:p.Gly143=
|
|
ENST00000419967.5:c.429C>T
|
ENSP00000405166.2:p.Gly143=
|
|
ENST00000445124.5:c.429C>T
|
ENSP00000408980.1:p.Gly143=
|
|
ENST00000445811.5:c.429C>T
|
ENSP00000395894.1:p.Gly143=
|
|
ENST00000447810.5:c.429C>T
|
ENSP00000395089.1:p.Gly143=
|
|
ENST00000466404.5:n.299C>T
|
|
|
ENST00000498612.1:n.212C>T
|
|
|
XM_006723137.2:c.429C>T
|
XP_006723200.1:p.Gly143=
|
|
XM_006723137.4:c.429C>T
|
XP_006723200.1:p.Gly143=
|
|
XR_002958293.1:n.559C>T
|
|
|
XR_935789.1:n.478C>T
|
|
|
XR_935789.3:n.490C>T
|
|