|
ENST00000359003.7:c.5781C>A
MANE Select
|
ENSP00000351894.2:p.Ile1927=
|
|
|
ENST00000359003.6:c.5781C>A
|
ENSP00000351894.2:p.Ile1927=
|
|
|
ENST00000374796.6:c.5781C>A
|
ENSP00000363929.2:p.Ile1927=
|
|
|
ENST00000612493.4:c.2915-3717C>A
|
ENSP00000481177.1:n.2915-3717C>A
|
|
|
ENST00000616167.1:c.2915-1543C>A
|
ENSP00000481935.1:n.2915-1543C>A
|
|
|
ENST00000628752.2:c.303-3717C>A
|
|
|
|
NM_001242539.1:c.2915-3717C>A
|
NP_001229468.1:n.2915-3717C>A
|
|
|
NM_014071.3:c.5781C>A
|
NP_054790.2:p.Ile1927=
|
|
|
XM_006723755.2:c.5781C>A
|
XP_006723818.1:p.Ile1927=
|
|
|
XM_011528721.1:c.5796C>A
|
XP_011527023.1:p.Ile1932=
|
|
|
XM_011528722.1:c.5796C>A
|
XP_011527024.1:p.Ile1932=
|
|
|
XM_011528723.1:c.5796C>A
|
XP_011527025.1:p.Ile1932=
|
|
|
XM_011528724.1:c.5796C>A
|
XP_011527026.1:p.Ile1932=
|
|
|
XM_011528725.1:c.5781C>A
|
XP_011527027.1:p.Ile1927=
|
|
|
XM_011528726.1:c.5763C>A
|
XP_011527028.1:p.Ile1921=
|
|
|
XM_011528727.1:c.5760C>A
|
XP_011527029.1:p.Ile1920=
|
|
|
XM_011528728.1:c.5796C>A
|
XP_011527030.1:p.Ile1932=
|
|
|
XM_011528729.1:c.5652C>A
|
XP_011527031.1:p.Ile1884=
|
|
|
XM_011528730.1:c.5796C>A
|
XP_011527032.1:p.Ile1932=
|
|
|
XM_011528731.1:c.5256C>A
|
XP_011527033.1:p.Ile1752=
|
|
|
XM_011528732.1:c.4713+1083C>A
|
XP_011527034.1:n.4713+1083C>A
|
|
|
XM_011528733.1:c.4713+1083C>A
|
XP_011527035.1:n.4713+1083C>A
|
|
|
XM_011528734.1:c.4713+1083C>A
|
XP_011527036.1:n.4713+1083C>A
|
|
|
XM_011528735.1:c.2930-3717C>A
|
XP_011527037.1:n.2930-3717C>A
|
|
|
XR_936514.1:n.4984+1083C>A
|
|
|
|
XR_936515.1:n.4984+1083C>A
|
|
|
|
NM_001242539.2:c.2915-3717C>A
|
NP_001229468.1:n.2915-3717C>A
|
|
|
NM_001318240.1:c.5781C>A
|
NP_001305169.1:p.Ile1927=
|
|
|
NM_014071.4:c.5781C>A
|
NP_054790.2:p.Ile1927=
|
|
|
XM_006723755.3:c.5781C>A
|
XP_006723818.1:p.Ile1927=
|
|
|
XM_011528721.3:c.5796C>A
|
XP_011527023.1:p.Ile1932=
|
|
|
XM_011528726.3:c.5763C>A
|
XP_011527028.1:p.Ile1921=
|
|
|
XM_011528727.3:c.5760C>A
|
XP_011527029.1:p.Ile1920=
|
|
|
XM_017027739.1:c.5853C>A
|
XP_016883228.1:p.Ile1951=
|
|
|
XM_017027740.2:c.5853C>A
|
XP_016883229.1:p.Ile1951=
|
|
|
XM_017027741.1:c.5853C>A
|
XP_016883230.1:p.Ile1951=
|
|
|
XM_017027742.2:c.5838C>A
|
XP_016883231.1:p.Ile1946=
|
|
|
XM_017027743.2:c.5853C>A
|
XP_016883232.1:p.Ile1951=
|
|
|
XM_017027744.2:c.5745C>A
|
XP_016883233.1:p.Ile1915=
|
|
|
XM_017027745.2:c.5709C>A
|
XP_016883234.1:p.Ile1903=
|
|
|
XM_017027746.1:c.5853C>A
|
XP_016883235.1:p.Ile1951=
|
|
|
XM_017027747.2:c.5313C>A
|
XP_016883236.1:p.Ile1771=
|
|
|
XM_017027748.1:c.4770+1083C>A
|
XP_016883237.1:n.4770+1083C>A
|
|
|
XM_017027749.1:c.4770+1083C>A
|
XP_016883238.1:n.4770+1083C>A
|
|
|
XM_017027750.2:c.2987-3717C>A
|
XP_016883239.1:n.2987-3717C>A
|
|
|
XM_017027751.1:c.2915-3717C>A
|
XP_016883240.1:n.2915-3717C>A
|
|
|
XR_001754214.2:n.5041+1083C>A
|
|
|
|
XR_001754215.2:n.5041+1083C>A
|
|
|
|
NM_014071.5:c.5781C>A
MANE Select
|
NP_054790.2:p.Ile1927=
|
|
