ENST00000358691.10:c.3249A=
MANE Select
|
ENSP00000351524.5:p.Glu1083=
|
|
ENST00000358691.9:c.3249A=
|
ENSP00000351524.5:p.Glu1083=
|
|
ENST00000579953.5:c.3252A=
|
ENSP00000463727.1:p.Glu1084=
|
|
ENST00000580168.5:c.3252A=
|
ENSP00000464512.1:p.Glu1084=
|
|
NM_014877.3:c.3249A=
|
NP_055692.2:p.Glu1083=
|
|
XM_005257888.3:c.3330A=
|
XP_005257945.1:p.Glu1110=
|
|
XM_005257889.3:c.3252A=
|
XP_005257946.1:p.Glu1084=
|
|
XM_005257890.3:c.3228A=
|
XP_005257947.1:p.Glu1076=
|
|
XM_006722214.2:c.3333A=
|
XP_006722277.1:p.Glu1111=
|
|
XM_006722215.2:c.2628A=
|
XP_006722278.1:p.Glu876=
|
|
XM_006722216.2:c.2157A=
|
XP_006722279.1:p.Glu719=
|
|
XM_011525544.1:c.3333A=
|
XP_011523846.1:p.Glu1111=
|
|
XM_011525545.1:c.3333A=
|
XP_011523847.1:p.Glu1111=
|
|
XR_934629.1:n.3324A=
|
|
|
NM_001330447.1:c.3252A=
|
NP_001317376.1:p.Glu1084=
|
|
XM_005257888.5:c.3330A=
|
XP_005257945.1:p.Glu1110=
|
|
XM_006722214.4:c.3333A=
|
XP_006722277.1:p.Glu1111=
|
|
XM_006722215.3:c.2628A=
|
XP_006722278.1:p.Glu876=
|
|
XM_006722216.3:c.2157A=
|
XP_006722279.1:p.Glu719=
|
|
XM_011525544.2:c.3333A=
|
XP_011523846.1:p.Glu1111=
|
|
XM_017025477.2:c.2544A=
|
XP_016880966.1:p.Glu848=
|
|
XM_017025478.1:c.2076A=
|
XP_016880967.1:p.Glu692=
|
|
XR_001752712.2:n.3424A=
|
|
|
XR_001752713.2:n.3276A=
|
|
|
XR_001752714.2:n.3192A=
|
|
|
NM_014877.4:c.3249A=
MANE Select
|
NP_055692.3:p.Glu1083=
|
|
NM_001330447.2:c.3252A=
|
NP_001317376.2:p.Glu1084=
|
|