|
ENST00000509514.6:c.509G>A
|
ENSP00000426272.2:p.Gly170Asp
|
|
|
ENST00000518349.6:c.113-17635G>A
|
ENSP00000507185.1:n.113-17635G>A
|
|
|
ENST00000682445.1:c.*390G>A
|
ENSP00000508061.1:n.*390G>A
|
|
|
ENST00000682531.1:n.610G>A
|
|
|
|
ENST00000682626.1:c.*15G>A
|
ENSP00000507857.1:n.*15G>A
|
|
|
ENST00000682996.1:c.509G>A
|
ENSP00000507792.1:p.Gly170Asp
|
|
|
ENST00000683265.1:n.602G>A
|
|
|
|
ENST00000683371.1:c.*639G>A
|
ENSP00000508376.1:n.*639G>A
|
|
|
ENST00000683390.1:n.2199G>A
|
|
|
|
ENST00000683549.1:n.430G>A
|
|
|
|
ENST00000683936.1:c.*394G>A
|
ENSP00000507721.1:n.*394G>A
|
|
|
ENST00000683974.1:n.591G>A
|
|
|
|
ENST00000683996.1:c.98G>A
|
ENSP00000507060.1:p.Gly33Asp
|
|
|
ENST00000684131.1:n.348G>A
|
|
|
|
ENST00000684160.1:c.*199G>A
|
ENSP00000507821.1:n.*199G>A
|
|
|
ENST00000684214.1:c.509G>A
|
ENSP00000508071.1:p.Gly170Asp
|
|
|
ENST00000414835.7:c.584G>A
|
ENSP00000411960.3:p.Gly195Asp
|
|
|
ENST00000510025.7:c.509G>A
MANE Select
|
ENSP00000424940.3:p.Gly170Asp
|
|
|
ENST00000643250.1:c.*381G>A
|
ENSP00000494737.1:n.*381G>A
|
|
|
ENST00000644146.1:c.*87G>A
|
ENSP00000494808.1:n.*87G>A
|
|
|
ENST00000645099.1:c.68G>A
|
ENSP00000496091.1:p.Gly23Asp
|
|
|
ENST00000645702.1:c.98G>A
|
ENSP00000496432.1:p.Gly33Asp
|
|
|
ENST00000645832.1:c.*394G>A
|
ENSP00000494316.1:n.*394G>A
|
|
|
ENST00000646058.1:c.509G>A
|
ENSP00000493579.1:p.Gly170Asp
|
|
|
ENST00000646355.1:c.*515G>A
|
ENSP00000493801.1:n.*515G>A
|
|
|
ENST00000646554.1:c.*487G>A
|
ENSP00000494542.1:n.*487G>A
|
|
|
ENST00000647335.1:c.*476G>A
|
ENSP00000495180.1:n.*476G>A
|
|
|
ENST00000647342.1:c.*440G>A
|
ENSP00000494992.1:n.*440G>A
|
|
|
ENST00000256216.10:c.509G>A
|
ENSP00000256216.6:p.Gly170Asp
|
|
|
ENST00000414835.6:c.89G>A
|
ENSP00000411960.2:p.Gly30Asp
|
|
|
ENST00000442060.7:c.509G>A
|
ENSP00000390208.3:p.Gly170Asp
|
|
|
ENST00000503168.5:n.498G>A
|
|
|
|
ENST00000504811.5:c.584G>A
|
ENSP00000420914.1:p.Gly195Asp
|
|
|
ENST00000505181.5:n.212G>A
|
|
|
|
ENST00000508788.5:n.411G>A
|
|
|
|
ENST00000509514.5:c.-376G>A
|
ENSP00000426272.1:n.-376G>A
|
|
|
ENST00000510025.5:c.437G>A
|
ENSP00000424940.1:p.Gly146Asp
|
|
|
ENST00000512644.1:n.77G>A
|
|
|
|
ENST00000512841.5:n.557G>A
|
|
|
|
ENST00000513628.5:c.98G>A
|
ENSP00000425993.1:p.Gly33Asp
|
|
|
ENST00000515235.6:n.569G>A
|
|
|
|
ENST00000515320.5:c.455G>A
|
ENSP00000424613.1:p.Gly152Asp
|
|
|
NM_000414.3:c.509G>A
|
NP_000405.1:p.Gly170Asp
|
|
|
NM_001199291.2:c.584G>A
|
NP_001186220.1:p.Gly195Asp
|
|
|
NM_001199292.1:c.455G>A
|
NP_001186221.1:p.Gly152Asp
|
|
|
NM_001292027.1:c.437G>A
|
NP_001278956.1:p.Gly146Asp
|
|
|
NM_001292028.1:c.89G>A
|
NP_001278957.1:p.Gly30Asp
|
|
|
NM_000414.4:c.509G>A
MANE Select
|
NP_000405.1:p.Gly170Asp
|
|
|
NM_001199291.3:c.584G>A
|
NP_001186220.1:p.Gly195Asp
|
|
|
NM_001199292.2:c.455G>A
|
NP_001186221.1:p.Gly152Asp
|
|
|
NM_001292027.2:c.437G>A
|
NP_001278956.1:p.Gly146Asp
|
|
|
NM_001292028.2:c.89G>A
|
NP_001278957.1:p.Gly30Asp
|
|
|
NM_001374497.1:c.500G>A
|
NP_001361426.1:p.Gly167Asp
|
|
|
NM_001374498.1:c.509G>A
|
NP_001361427.1:p.Gly170Asp
|
|
|
NM_001374499.1:c.182G>A
|
NP_001361428.1:p.Gly61Asp
|
|
|
NM_001374500.1:c.68G>A
|
NP_001361429.1:p.Gly23Asp
|
|
|
NM_001374501.1:c.98G>A
|
NP_001361430.1:p.Gly33Asp
|
|
|
NM_001374502.1:c.98G>A
|
NP_001361431.1:p.Gly33Asp
|
|
|
NM_001374503.1:c.98G>A
|
NP_001361432.1:p.Gly33Asp
|
|
|
NR_164653.1:n.588G>A
|
|
|
|
NR_164654.1:n.776G>A
|
|
|
