ENST00000505435.4:n.871A>G
|
|
|
ENST00000505787.8:n.2755A>G
|
|
|
ENST00000509358.7:c.915A>G
|
ENSP00000420994.3:p.Glu305=
|
|
ENST00000509539.3:c.177A>G
|
ENSP00000425474.3:p.Glu59=
|
|
ENST00000510895.7:n.1038A>G
|
|
|
ENST00000629193.3:c.801A>G
|
ENSP00000486535.2:p.Glu267=
|
|
ENST00000681968.1:c.408A>G
|
ENSP00000508143.1:p.Glu136=
|
|
ENST00000682045.1:c.771A>G
|
ENSP00000507329.1:p.Glu257=
|
|
ENST00000682214.1:c.522A>G
|
ENSP00000507336.1:p.Glu174=
|
|
ENST00000682499.1:n.1736A>G
|
|
|
ENST00000682541.1:c.915A>G
|
ENSP00000507673.1:p.Glu305=
|
|
ENST00000682687.1:c.915A>G
|
ENSP00000507945.1:p.Glu305=
|
|
ENST00000682727.1:c.915A>G
|
ENSP00000507393.1:p.Glu305=
|
|
ENST00000682876.1:c.1044A>G
|
ENSP00000508389.1:p.Glu348=
|
|
ENST00000683098.1:c.803+2977A>G
|
ENSP00000507670.1:n.803+2977A>G
|
|
ENST00000683258.1:c.*636A>G
|
ENSP00000507448.1:n.*636A>G
|
|
ENST00000683339.1:c.699A>G
|
ENSP00000507758.1:p.Glu233=
|
|
ENST00000683403.1:c.825A>G
|
ENSP00000507896.1:p.Glu275=
|
|
ENST00000683429.1:c.522A>G
|
ENSP00000507697.1:p.Glu174=
|
|
ENST00000683665.1:c.915A>G
|
ENSP00000507068.1:p.Glu305=
|
|
ENST00000683789.1:c.801A>G
|
ENSP00000507012.1:p.Glu267=
|
|
ENST00000683847.1:n.759A>G
|
|
|
ENST00000683882.1:c.915A>G
|
ENSP00000506735.1:p.Glu305=
|
|
ENST00000684024.1:c.*586A>G
|
ENSP00000507175.1:n.*586A>G
|
|
ENST00000684254.1:c.*641A>G
|
ENSP00000508001.1:n.*641A>G
|
|
ENST00000684310.1:c.165+120A>G
|
ENSP00000507550.1:n.165+120A>G
|
|
ENST00000684530.1:c.177A>G
|
ENSP00000507439.1:p.Glu59=
|
|
ENST00000684652.1:n.1917A>G
|
|
|
ENST00000340941.11:c.915A>G
MANE Select
|
ENSP00000343657.6:p.Glu305=
|
|
ENST00000340941.10:c.915A>G
|
ENSP00000343657.6:p.Glu305=
|
|
ENST00000505435.3:n.266A>G
|
|
|
ENST00000509358.6:c.915A>G
|
ENSP00000420994.2:p.Glu305=
|
|
ENST00000509539.2:c.240A>G
|
ENSP00000425474.2:p.Glu80=
|
|
ENST00000510895.6:n.529A>G
|
|
|
ENST00000512218.6:c.801A>G
|
ENSP00000423202.2:p.Glu267=
|
|
ENST00000629193.2:c.801A>G
|
ENSP00000486535.1:p.Glu267=
|
|
NM_022132.4:c.915A>G
|
NP_071415.1:p.Glu305=
|
|
XM_005248567.1:c.801A>G
|
XP_005248624.1:p.Glu267=
|
|
XM_011543528.1:c.915A>G
|
XP_011541830.1:p.Glu305=
|
|
XM_011543529.1:c.915A>G
|
XP_011541831.1:p.Glu305=
|
|
NM_001363147.1:c.801A>G
|
NP_001350076.1:p.Glu267=
|
|
XM_011543529.2:c.915A>G
|
XP_011541831.1:p.Glu305=
|
|
XM_017009688.1:c.915A>G
|
XP_016865177.1:p.Glu305=
|
|
XR_001742172.1:n.955A>G
|
|
|
NM_022132.5:c.915A>G
MANE Select
|
NP_071415.1:p.Glu305=
|
|