ENST00000388913.4:c.1166A=
MANE Select
|
ENSP00000373565.3:p.Glu389=
|
|
ENST00000650760.1:c.1769A=
|
ENSP00000499217.1:p.Glu590=
|
|
ENST00000388913.3:c.1166A=
|
ENSP00000373565.3:p.Glu389=
|
|
ENST00000395103.2:c.346A=
|
|
|
NM_198488.3:c.1166A=
|
NP_940890.3:p.Glu389=
|
|
XM_005250887.2:c.1223A=
|
XP_005250944.1:p.Glu408=
|
|
XM_005250888.2:c.1184A=
|
XP_005250945.1:p.Glu395=
|
|
XM_005250889.2:c.1166A=
|
XP_005250946.1:p.Glu389=
|
|
XM_011516980.1:c.1487A=
|
XP_011515282.1:p.Glu496=
|
|
XM_011516981.1:c.1334A=
|
XP_011515283.1:p.Glu445=
|
|
XM_005250887.3:c.1223A=
|
XP_005250944.1:p.Glu408=
|
|
XM_005250888.3:c.1184A=
|
XP_005250945.1:p.Glu395=
|
|
XM_005250889.3:c.1166A=
|
XP_005250946.1:p.Glu389=
|
|
XM_011516980.2:c.1769A=
|
XP_011515282.2:p.Glu590=
|
|
XM_011516981.2:c.1334A=
|
XP_011515283.1:p.Glu445=
|
|
XM_024447131.1:c.1166A=
|
XP_024302899.1:p.Glu389=
|
|
NM_198488.4:c.1166A=
|
NP_940890.3:p.Glu389=
|
|
NM_198488.5:c.1166A=
MANE Select
|
NP_940890.4:p.Glu389=
|
|