ENST00000368666.7:c.252A>G
MANE Select
|
ENSP00000357655.4:p.Glu84=
|
|
ENST00000639360.1:c.156A>G
|
ENSP00000491774.1:p.Glu52=
|
|
ENST00000230529.9:c.252A>G
|
ENSP00000230529.5:p.Glu84=
|
|
ENST00000361714.5:c.252A>G
|
ENSP00000354734.2:p.Glu84=
|
|
ENST00000368663.4:c.252A>G
|
ENSP00000357652.4:p.Glu84=
|
|
ENST00000368664.7:c.306A>G
|
ENSP00000357653.3:p.Glu102=
|
|
ENST00000368666.6:c.306A>G
|
ENSP00000357655.3:p.Glu102=
|
|
ENST00000409166.5:c.-507-85A>G
|
ENSP00000386467.1:n.-507-85A>G
|
|
ENST00000454589.5:c.252A>G
|
ENSP00000395928.1:p.Glu84=
|
|
ENST00000604763.5:c.252A>G
|
ENSP00000473777.1:p.Glu84=
|
|
ENST00000620524.3:n.186A>G
|
|
|
NM_003880.3:c.252A>G
|
NP_003871.1:p.Glu84=
|
|
NM_198239.1:c.306A>G
|
NP_937882.1:p.Glu102=
|
|
NR_125353.1:n.442A>G
|
|
|
NR_125354.1:n.362A>G
|
|
|
XM_011536220.1:c.252A>G
|
XP_011534522.1:p.Glu84=
|
|
XM_011536221.1:c.315A>G
|
XP_011534523.1:p.Glu105=
|
|
XM_011536222.1:c.390A>G
|
XP_011534524.1:p.Glu130=
|
|
XM_011536222.2:c.315A>G
|
XP_011534524.2:p.Glu105=
|
|
XR_001743705.1:n.790A>G
|
|
|
NM_003880.4:c.252A>G
|
NP_003871.1:p.Glu84=
|
|
NM_198239.2:c.252A>G
MANE Select
|
NP_937882.2:p.Glu84=
|
|
NR_125353.2:n.506A>G
|
|
|
NR_125354.3:n.333A>G
|
|
|