ENST00000474381.2:n.2878A>G
|
|
|
ENST00000481849.6:n.2304A>G
|
|
|
ENST00000497377.6:n.2304A>G
|
|
|
ENST00000640094.2:c.831A>G
|
ENSP00000491275.2:p.Glu277=
|
|
ENST00000696558.1:c.900A>G
|
ENSP00000512716.1:n.900A>G
|
|
ENST00000696559.1:c.831A>G
|
ENSP00000512717.1:p.Glu277=
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|
ENST00000696560.1:c.831A>G
|
ENSP00000512718.1:p.Glu277=
|
|
ENST00000696561.1:c.831A>G
|
ENSP00000512719.1:p.Glu277=
|
|
ENST00000696562.1:c.831A>G
|
ENSP00000512720.1:p.Glu277=
|
|
ENST00000412585.7:c.831A>G
MANE Select
|
ENSP00000399168.2:p.Glu277=
|
|
ENST00000640094.1:c.24A>G
|
ENSP00000491275.1:p.Glu8=
|
|
ENST00000412585.6:c.831A>G
|
ENSP00000399168.2:p.Glu277=
|
|
ENST00000463574.1:n.422A>G
|
|
|
NM_005514.6:c.831A>G
|
NP_005505.2:p.Glu277=
|
|
XM_011514556.1:c.864A>G
|
XP_011512858.1:p.Glu288=
|
|
XM_011514557.1:c.831A>G
|
XP_011512859.1:p.Glu277=
|
|
XR_926175.1:n.1270A>G
|
|
|
NM_005514.7:c.831A>G
|
NP_005505.2:p.Glu277=
|
|
NM_005514.8:c.831A>G
MANE Select
|
NP_005505.2:p.Glu277=
|
|