|
ENST00000370841.9:c.894A>C
MANE Select
|
ENSP00000359878.5:p.Glu298Asp
|
|
|
ENST00000473018.3:n.3018A>C
|
|
|
|
ENST00000532207.6:n.1783A>C
|
|
|
|
ENST00000541113.6:c.849+936A>C
|
ENSP00000442324.2:n.849+936A>C
|
|
|
ENST00000679509.1:n.1856A>C
|
|
|
|
ENST00000679530.1:c.*662A>C
|
ENSP00000506454.1:n.*662A>C
|
|
|
ENST00000679615.1:n.2909A>C
|
|
|
|
ENST00000679687.1:c.456A>C
|
ENSP00000506598.1:p.Glu152Asp
|
|
|
ENST00000679704.1:c.*660A>C
|
ENSP00000505117.1:n.*660A>C
|
|
|
ENST00000679709.1:c.*857A>C
|
ENSP00000506623.1:n.*857A>C
|
|
|
ENST00000679976.1:c.*478A>C
|
ENSP00000505565.1:n.*478A>C
|
|
|
ENST00000680166.1:n.4183A>C
|
|
|
|
ENST00000680315.1:n.777A>C
|
|
|
|
ENST00000680517.1:c.*282A>C
|
ENSP00000505803.1:n.*282A>C
|
|
|
ENST00000680582.1:n.1856A>C
|
|
|
|
ENST00000680613.1:c.*265A>C
|
ENSP00000506114.1:n.*265A>C
|
|
|
ENST00000680662.1:c.*808A>C
|
ENSP00000505080.1:n.*808A>C
|
|
|
ENST00000680691.1:c.*557A>C
|
ENSP00000506487.1:n.*557A>C
|
|
|
ENST00000680694.1:c.*482A>C
|
ENSP00000505658.1:n.*482A>C
|
|
|
ENST00000680743.1:c.*561A>C
|
ENSP00000505073.1:n.*561A>C
|
|
|
ENST00000680749.1:c.*179A>C
|
ENSP00000505122.1:n.*179A>C
|
|
|
ENST00000680798.1:c.*369A>C
|
ENSP00000505670.1:n.*369A>C
|
|
|
ENST00000680805.1:c.753A>C
|
ENSP00000505447.1:p.Glu251Asp
|
|
|
ENST00000680844.1:c.*678A>C
|
ENSP00000506541.1:n.*678A>C
|
|
|
ENST00000680948.1:c.*761A>C
|
ENSP00000505441.1:n.*761A>C
|
|
|
ENST00000680964.1:c.894A>C
|
ENSP00000505961.1:p.Glu298Asp
|
|
|
ENST00000681037.1:c.*2378A>C
|
ENSP00000506025.1:n.*2378A>C
|
|
|
ENST00000681063.1:c.*41A>C
|
ENSP00000506616.1:n.*41A>C
|
|
|
ENST00000681209.1:c.*549A>C
|
ENSP00000505877.1:n.*549A>C
|
|
|
ENST00000681278.1:n.1251A>C
|
|
|
|
ENST00000681289.1:n.4889A>C
|
|
|
|
ENST00000681361.1:c.*561A>C
|
ENSP00000506679.1:n.*561A>C
|
|
|
ENST00000681430.1:c.894A>C
|
ENSP00000506301.1:p.Glu298Asp
|
|
|
ENST00000681446.1:c.*476A>C
|
ENSP00000506244.1:n.*476A>C
|
|
|
ENST00000681450.1:c.*565A>C
|
ENSP00000505660.1:n.*565A>C
|
|
|
ENST00000681548.1:c.*480A>C
|
ENSP00000505275.1:n.*480A>C
|
|
|
ENST00000681616.1:c.*553A>C
|
ENSP00000505111.1:n.*553A>C
|
|
|
ENST00000681621.1:c.*478A>C
|
ENSP00000505770.1:n.*478A>C
|
|
|
ENST00000681680.1:n.2989A>C
|
|
|
|
ENST00000681720.1:c.*349A>C
|
ENSP00000505438.1:n.*349A>C
|
|
|
ENST00000681730.1:n.1116A>C
|
|
|
|
ENST00000681790.1:c.636A>C
|
ENSP00000505130.1:p.Glu212Asp
|
|
|
ENST00000681837.1:n.1510A>C
|
|
|
|
ENST00000681913.1:n.3018A>C
|
|
|
|
ENST00000681916.1:c.*662A>C
|
ENSP00000506477.1:n.*662A>C
|
|
|
ENST00000681930.1:n.3018A>C
|
|
|
|
ENST00000370834.9:c.993A>C
|
ENSP00000359871.5:p.Glu331Asp
|
|
|
ENST00000370841.8:c.894A>C
|
ENSP00000359878.4:p.Glu298Asp
|
|
|
ENST00000420607.6:c.906A>C
|
ENSP00000409612.2:p.Glu302Asp
|
|
|
ENST00000481374.1:n.45A>C
|
|
|
|
ENST00000525808.5:c.*480A>C
|
ENSP00000434823.1:n.*480A>C
|
|
|
ENST00000526129.5:c.*678A>C
|
ENSP00000434092.1:n.*678A>C
|
|
|
ENST00000526196.5:c.*662A>C
|
ENSP00000431953.1:n.*662A>C
|
|
|
ENST00000528016.1:c.108A>C
|
ENSP00000434284.1:p.Glu36Asp
|
|
|
ENST00000529059.5:n.803A>C
|
|
|
|
ENST00000532207.5:n.624A>C
|
|
|
|
ENST00000534334.5:c.*478A>C
|
ENSP00000435584.1:n.*478A>C
|
|
|
ENST00000541113.5:c.786A>C
|
ENSP00000442324.1:p.Glu262Asp
|
|
|
NM_000016.5:c.894A>C
|
NP_000007.1:p.Glu298Asp
|
|
|
NM_001127328.2:c.906A>C
|
NP_001120800.1:p.Glu302Asp
|
|
|
NM_001286042.1:c.786A>C
|
NP_001272971.1:p.Glu262Asp
|
|
|
NM_001286043.1:c.993A>C
|
NP_001272972.1:p.Glu331Asp
|
|
|
NM_001286044.1:c.327A>C
|
NP_001272973.1:p.Glu109Asp
|
|
|
NM_000016.6:c.894A>C
MANE Select
|
NP_000007.1:p.Glu298Asp
|
|
|
NM_001127328.3:c.906A>C
|
NP_001120800.1:p.Glu302Asp
|
|
|
NM_001286042.2:c.786A>C
|
NP_001272971.1:p.Glu262Asp
|
|
|
NM_001286043.2:c.993A>C
|
NP_001272972.1:p.Glu331Asp
|
|
|
NM_001286044.2:c.327A>C
|
NP_001272973.1:p.Glu109Asp
|
|
