ENST00000381733.9:c.821A>T
|
ENSP00000371152.4:p.Glu274Val
|
|
ENST00000518746.2:n.2459A>T
|
|
|
ENST00000520781.6:c.698A>T
|
ENSP00000427751.1:p.Glu233Val
|
|
ENST00000521542.2:n.81A>T
|
|
|
ENST00000635756.1:c.186A>T
|
|
|
ENST00000635944.1:c.*609A>T
|
ENSP00000490195.1:n.*609A>T
|
|
ENST00000635998.1:c.773A>T
|
ENSP00000490506.1:p.Glu258Val
|
|
ENST00000636009.1:c.630A>T
|
ENSP00000489988.1:n.630A>T
|
|
ENST00000636033.1:c.*609A>T
|
ENSP00000489617.1:n.*609A>T
|
|
ENST00000636050.1:c.*616A>T
|
ENSP00000490562.1:n.*616A>T
|
|
ENST00000636128.1:c.452A>T
|
ENSP00000489789.1:p.Glu151Val
|
|
ENST00000636160.1:c.*665A>T
|
ENSP00000489651.1:n.*665A>T
|
|
ENST00000636171.1:c.716A>T
|
ENSP00000489761.1:p.Glu239Val
|
|
ENST00000636455.1:c.821A>T
|
ENSP00000490502.1:p.Glu274Val
|
|
ENST00000636494.1:c.*553A>T
|
ENSP00000490388.1:n.*553A>T
|
|
ENST00000636563.1:n.435A>T
|
|
|
ENST00000636577.1:c.713A>T
|
ENSP00000490027.1:p.Glu238Val
|
|
ENST00000636691.1:c.578A>T
|
ENSP00000490725.1:p.Glu193Val
|
|
ENST00000636701.1:c.*424A>T
|
ENSP00000489800.1:n.*424A>T
|
|
ENST00000636815.1:c.690A>T
|
|
|
ENST00000636920.1:c.*609A>T
|
ENSP00000490437.1:n.*609A>T
|
|
ENST00000636997.1:c.686A>T
|
ENSP00000490093.1:p.Glu229Val
|
|
ENST00000637013.1:c.*1141A>T
|
ENSP00000490596.1:n.*1141A>T
|
|
ENST00000637014.1:n.1180A>T
|
|
|
ENST00000637095.1:c.*553A>T
|
ENSP00000490415.1:n.*553A>T
|
|
ENST00000637244.1:c.*1291A>T
|
ENSP00000490188.1:n.*1291A>T
|
|
ENST00000637343.1:n.2210A>T
|
|
|
ENST00000637429.1:c.*985A>T
|
ENSP00000490522.1:n.*985A>T
|
|
ENST00000637484.1:c.*735A>T
|
ENSP00000490837.1:n.*735A>T
|
|
ENST00000637528.1:c.710A>T
|
ENSP00000490801.1:p.Glu237Val
|
|
ENST00000637609.1:n.3494A>T
|
|
|
ENST00000637636.1:c.767A>T
|
ENSP00000490112.1:p.Glu256Val
|
|
ENST00000637790.2:c.773A>T
MANE Select
|
ENSP00000490272.1:p.Glu258Val
|
|
ENST00000637857.1:n.1139A>T
|
|
|
ENST00000637922.1:c.578A>T
|
ENSP00000490071.1:p.Glu193Val
|
|
ENST00000637991.1:c.746A>T
|
ENSP00000489901.1:p.Glu249Val
|
|
ENST00000638028.1:n.990A>T
|
|
|
ENST00000638069.1:n.1594A>T
|
|
|
ENST00000262097.10:c.773A>T
|
ENSP00000262097.6:p.Glu258Val
|
|
ENST00000314146.10:c.755A>T
|
ENSP00000326970.10:p.Glu252Val
|
|
ENST00000381733.8:c.821A>T
|
ENSP00000371152.4:p.Glu274Val
|
|
ENST00000519468.5:n.602A>T
|
|
|
ENST00000520781.5:c.698A>T
|
ENSP00000427751.1:p.Glu233Val
|
|
ENST00000521542.1:n.486A>T
|
|
|
NM_001127505.1:c.755A>T
|
NP_001120977.1:p.Glu252Val
|
|
NM_001127505.2:c.755A>T
|
NP_001120977.1:p.Glu252Val
|
|
NM_004315.4:c.821A>T
|
NP_004306.3:p.Glu274Val
|
|
NM_004315.5:c.821A>T
|
NP_004306.3:p.Glu274Val
|
|
NM_177924.3:c.773A>T
|
NP_808592.2:p.Glu258Val
|
|
NM_177924.4:c.773A>T
|
NP_808592.2:p.Glu258Val
|
|
XM_005273504.2:c.707A>T
|
XP_005273561.1:p.Glu236Val
|
|
NM_001363743.1:c.578A>T
|
NP_001350672.1:p.Glu193Val
|
|
XM_005273504.3:c.707A>T
|
XP_005273561.1:p.Glu236Val
|
|
NM_177924.5:c.773A>T
MANE Select
|
NP_808592.2:p.Glu258Val
|
|
NM_001127505.3:c.755A>T
|
NP_001120977.1:p.Glu252Val
|
|
NM_001363743.2:c.578A>T
|
NP_001350672.1:p.Glu193Val
|
|
NM_004315.6:c.821A>T
|
NP_004306.3:p.Glu274Val
|
|