ENST00000265104.5:c.9732A>G
MANE Select
|
ENSP00000265104.4:p.Glu3244=
|
|
ENST00000681290.1:c.9687A>G
|
ENSP00000505288.1:p.Glu3229=
|
|
ENST00000265104.4:c.9732A>G
|
ENSP00000265104.4:p.Glu3244=
|
|
ENST00000504001.3:n.444A>G
|
|
|
NM_001369.2:c.9732A>G
|
NP_001360.1:p.Glu3244=
|
|
XM_005248262.2:c.9687A>G
|
XP_005248319.1:p.Glu3229=
|
|
XM_005248262.3:c.9840A>G
|
XP_005248319.2:p.Glu3280=
|
|
XM_017009177.1:c.9840A>G
|
XP_016864666.1:p.Glu3280=
|
|
XM_017009178.1:c.8745A>G
|
XP_016864667.1:p.Glu2915=
|
|
XM_017009179.2:c.8745A>G
|
XP_016864668.1:p.Glu2915=
|
|
XM_017009180.1:c.9840A>G
|
XP_016864669.1:p.Glu3280=
|
|
XM_017009181.1:c.9840A>G
|
XP_016864670.1:p.Glu3280=
|
|
XM_017009182.1:c.9840A>G
|
XP_016864671.1:p.Glu3280=
|
|
XM_017009185.1:c.4929A>G
|
XP_016864674.1:p.Glu1643=
|
|
XM_017009186.1:c.4482A>G
|
XP_016864675.1:p.Glu1494=
|
|
XM_017009188.1:c.3819A>G
|
XP_016864677.1:p.Glu1273=
|
|
XM_024454388.1:c.8745A>G
|
XP_024310156.1:p.Glu2915=
|
|
XM_024454389.1:c.8334A>G
|
XP_024310157.1:p.Glu2778=
|
|
NM_001369.3:c.9732A>G
MANE Select
|
NP_001360.1:p.Glu3244=
|
|