|
ENST00000509977.2:n.647T>G
|
|
|
|
ENST00000510362.6:c.474T>G
|
ENSP00000425089.2:p.Asp158Glu
|
|
|
ENST00000682033.1:c.127-2429T>G
|
|
|
|
ENST00000682142.1:c.696T>G
|
ENSP00000506804.1:p.Asp232Glu
|
|
|
ENST00000682229.1:c.1155T>G
|
ENSP00000507342.1:p.Asp385Glu
|
|
|
ENST00000682564.1:c.996T>G
|
ENSP00000508099.1:p.Asp332Glu
|
|
|
ENST00000682628.1:c.474T>G
|
ENSP00000507536.1:p.Asp158Glu
|
|
|
ENST00000682982.1:n.1773T>G
|
|
|
|
ENST00000683045.1:n.5543T>G
|
|
|
|
ENST00000683130.1:c.*245T>G
|
ENSP00000507709.1:n.*245T>G
|
|
|
ENST00000683169.1:n.1498T>G
|
|
|
|
ENST00000683414.1:c.474T>G
|
ENSP00000508335.1:p.Asp158Glu
|
|
|
ENST00000683527.1:c.*298T>G
|
ENSP00000507253.1:n.*298T>G
|
|
|
ENST00000683539.1:c.474T>G
|
ENSP00000507466.1:p.Asp158Glu
|
|
|
ENST00000684456.1:c.-70T>G
|
ENSP00000508060.1:n.-70T>G
|
|
|
ENST00000684521.1:c.861T>G
|
ENSP00000507521.1:p.Asp287Glu
|
|
|
ENST00000684695.1:n.3269T>G
|
|
|
|
ENST00000306320.10:c.999T>G
MANE Select
|
ENSP00000304642.9:p.Asp333Glu
|
|
|
ENST00000306320.9:c.999T>G
|
ENSP00000304642.9:p.Asp333Glu
|
|
|
ENST00000399793.6:c.576T>G
|
ENSP00000382691.2:p.Asp192Glu
|
|
|
ENST00000509977.1:n.635T>G
|
|
|
|
ENST00000510362.5:c.158T>G
|
|
|
|
NM_001034850.2:c.999T>G , LRG_363t1:c.999T>G
|
NP_001030022.1:p.Asp333Glu
|
|
|
NM_019000.4:c.576T>G
|
NP_061873.2:p.Asp192Glu
|
|
|
XM_011514053.1:c.1119T>G
|
XP_011512355.1:p.Asp373Glu
|
|
|
XM_011514054.1:c.696T>G
|
XP_011512356.1:p.Asp232Glu
|
|
|
XM_011514055.1:c.600T>G
|
XP_011512357.1:p.Asp200Glu
|
|
|
XM_011514053.3:c.1119T>G
|
XP_011512355.1:p.Asp373Glu
|
|
|
XM_011514054.2:c.696T>G
|
XP_011512356.1:p.Asp232Glu
|
|
|
XM_011514055.3:c.600T>G
|
XP_011512357.1:p.Asp200Glu
|
|
|
XM_024446117.1:c.474T>G
|
XP_024301885.1:p.Asp158Glu
|
|
|
XM_024446118.1:c.474T>G
|
XP_024301886.1:p.Asp158Glu
|
|
|
NM_001034850.3:c.999T>G
MANE Select
|
NP_001030022.1:p.Asp333Glu
|
|
|
NM_019000.5:c.576T>G
|
NP_061873.2:p.Asp192Glu
|
|
