ENST00000267890.11:c.1285G=
MANE Select
|
ENSP00000267890.6:p.Glu429=
|
|
ENST00000267890.10:c.1285G=
|
ENSP00000267890.6:p.Glu429=
|
|
ENST00000567274.5:c.1180G=
|
ENSP00000457489.1:p.Glu394=
|
|
ENST00000567840.5:c.1285G=
|
ENSP00000455734.1:p.Glu429=
|
|
ENST00000622375.4:c.2500G=
|
ENSP00000479984.1:p.Glu834=
|
|
NM_173500.3:c.1285G=
|
NP_775771.3:p.Glu429=
|
|
XM_005254171.3:c.1303G=
|
XP_005254228.1:p.Glu435=
|
|
XM_005254173.3:c.1078G=
|
XP_005254230.1:p.Glu360=
|
|
XM_006720402.2:c.1270G=
|
XP_006720465.1:p.Glu424=
|
|
XM_006720403.2:c.1078G=
|
XP_006720466.1:p.Glu360=
|
|
XM_011521267.1:c.1078G=
|
XP_011519569.1:p.Glu360=
|
|
XM_011521268.1:c.1018G=
|
XP_011519570.1:p.Glu340=
|
|
XM_011521269.1:c.1006G=
|
XP_011519571.1:p.Glu336=
|
|
XM_005254171.5:c.1303G=
|
XP_005254228.1:p.Glu435=
|
|
XM_005254173.5:c.1078G=
|
XP_005254230.1:p.Glu360=
|
|
XM_006720402.4:c.1270G=
|
XP_006720465.1:p.Glu424=
|
|
XM_006720403.4:c.1078G=
|
XP_006720466.1:p.Glu360=
|
|
XM_017021950.2:c.1006G=
|
XP_016877439.1:p.Glu336=
|
|
XM_024449849.1:c.1285G=
|
XP_024305617.1:p.Glu429=
|
|
XM_024449850.1:c.1285G=
|
XP_024305618.1:p.Glu429=
|
|
XM_024449851.1:c.1078G=
|
XP_024305619.1:p.Glu360=
|
|
NM_173500.4:c.1285G=
MANE Select
|
NP_775771.3:p.Glu429=
|
|