ENST00000270301.12:c.4198G=
|
ENSP00000270301.6:p.Glu1400=
|
|
ENST00000401500.7:c.4213G=
MANE Select
|
ENSP00000384792.1:p.Glu1405=
|
|
ENST00000587391.6:c.*4073G=
|
ENSP00000465525.1:n.*4073G=
|
|
ENST00000679357.1:c.2293G=
|
|
|
ENST00000679598.1:c.958G=
|
|
|
ENST00000679682.1:c.4198G=
|
ENSP00000506226.1:p.Glu1400=
|
|
ENST00000679714.1:c.4207G=
|
ENSP00000506627.1:p.Glu1403=
|
|
ENST00000679757.1:c.3862G=
|
ENSP00000505158.1:p.Glu1288=
|
|
ENST00000679858.1:c.*3595G=
|
ENSP00000505655.1:n.*3595G=
|
|
ENST00000680211.1:c.814G=
|
ENSP00000506102.1:p.Glu272=
|
|
ENST00000680280.1:n.1716G=
|
|
|
ENST00000680349.1:n.2862G=
|
|
|
ENST00000680403.1:c.4198G=
|
ENSP00000505677.1:p.Glu1400=
|
|
ENST00000680564.1:c.3964G=
|
ENSP00000505582.1:p.Glu1322=
|
|
ENST00000680590.1:c.*2593G=
|
ENSP00000505350.1:n.*2593G=
|
|
ENST00000680597.1:c.946G=
|
|
|
ENST00000680739.1:c.1228G=
|
|
|
ENST00000680773.1:n.2714G=
|
|
|
ENST00000680806.1:c.*3516G=
|
ENSP00000506418.1:n.*3516G=
|
|
ENST00000680997.1:n.2145G=
|
|
|
ENST00000681608.1:n.2058G=
|
|
|
ENST00000681625.1:c.*1545G=
|
ENSP00000505555.1:n.*1545G=
|
|
ENST00000681648.1:n.2264G=
|
|
|
ENST00000270301.11:c.4198G=
|
ENSP00000270301.6:p.Glu1400=
|
|
ENST00000401500.6:c.4213G=
|
ENSP00000384792.1:p.Glu1405=
|
|
ENST00000587391.5:c.*4073G=
|
ENSP00000465525.1:n.*4073G=
|
|
NM_001083961.1:c.4213G=
|
NP_001077430.1:p.Glu1405=
|
|
NM_173636.4:c.4198G=
|
NP_775907.4:p.Glu1400=
|
|
XM_005258809.2:c.4102G=
|
XP_005258866.1:p.Glu1368=
|
|
XM_011526837.1:c.4198G=
|
XP_011525139.1:p.Glu1400=
|
|
XM_011526838.1:c.3964G=
|
XP_011525140.1:p.Glu1322=
|
|
XM_011526839.1:c.3862G=
|
XP_011525141.1:p.Glu1288=
|
|
XM_011526840.1:c.3205G=
|
XP_011525142.1:p.Glu1069=
|
|
XM_011526841.1:c.2791G=
|
XP_011525143.1:p.Glu931=
|
|
XM_011526842.1:c.2644G=
|
XP_011525144.1:p.Glu882=
|
|
XM_011526843.1:c.1960G=
|
XP_011525145.1:p.Glu654=
|
|
XM_011526844.1:c.1960G=
|
XP_011525146.1:p.Glu654=
|
|
XM_011526840.2:c.3205G=
|
XP_011525142.1:p.Glu1069=
|
|
XM_011526841.2:c.2791G=
|
XP_011525143.1:p.Glu931=
|
|
XM_011526844.2:c.1960G=
|
XP_011525146.1:p.Glu654=
|
|
XM_017026665.1:c.4213G=
|
XP_016882154.1:p.Glu1405=
|
|
NM_001083961.2:c.4213G=
MANE Select
|
NP_001077430.1:p.Glu1405=
|
|
NM_173636.5:c.4198G=
|
NP_775907.4:p.Glu1400=
|
|