|
ENST00000370841.9:c.892G>A
MANE Select
|
ENSP00000359878.5:p.Glu298Lys
|
|
|
ENST00000473018.3:n.3016G>A
|
|
|
|
ENST00000532207.6:n.1781G>A
|
|
|
|
ENST00000541113.6:c.849+934G>A
|
ENSP00000442324.2:n.849+934G>A
|
|
|
ENST00000679509.1:n.1854G>A
|
|
|
|
ENST00000679530.1:c.*660G>A
|
ENSP00000506454.1:n.*660G>A
|
|
|
ENST00000679615.1:n.2907G>A
|
|
|
|
ENST00000679687.1:c.454G>A
|
ENSP00000506598.1:p.Glu152Lys
|
|
|
ENST00000679704.1:c.*658G>A
|
ENSP00000505117.1:n.*658G>A
|
|
|
ENST00000679709.1:c.*855G>A
|
ENSP00000506623.1:n.*855G>A
|
|
|
ENST00000679976.1:c.*476G>A
|
ENSP00000505565.1:n.*476G>A
|
|
|
ENST00000680166.1:n.4181G>A
|
|
|
|
ENST00000680315.1:n.775G>A
|
|
|
|
ENST00000680517.1:c.*280G>A
|
ENSP00000505803.1:n.*280G>A
|
|
|
ENST00000680582.1:n.1854G>A
|
|
|
|
ENST00000680613.1:c.*263G>A
|
ENSP00000506114.1:n.*263G>A
|
|
|
ENST00000680662.1:c.*806G>A
|
ENSP00000505080.1:n.*806G>A
|
|
|
ENST00000680691.1:c.*555G>A
|
ENSP00000506487.1:n.*555G>A
|
|
|
ENST00000680694.1:c.*480G>A
|
ENSP00000505658.1:n.*480G>A
|
|
|
ENST00000680743.1:c.*559G>A
|
ENSP00000505073.1:n.*559G>A
|
|
|
ENST00000680749.1:c.*177G>A
|
ENSP00000505122.1:n.*177G>A
|
|
|
ENST00000680798.1:c.*367G>A
|
ENSP00000505670.1:n.*367G>A
|
|
|
ENST00000680805.1:c.751G>A
|
ENSP00000505447.1:p.Glu251Lys
|
|
|
ENST00000680844.1:c.*676G>A
|
ENSP00000506541.1:n.*676G>A
|
|
|
ENST00000680948.1:c.*759G>A
|
ENSP00000505441.1:n.*759G>A
|
|
|
ENST00000680964.1:c.892G>A
|
ENSP00000505961.1:p.Glu298Lys
|
|
|
ENST00000681037.1:c.*2376G>A
|
ENSP00000506025.1:n.*2376G>A
|
|
|
ENST00000681063.1:c.*39G>A
|
ENSP00000506616.1:n.*39G>A
|
|
|
ENST00000681209.1:c.*547G>A
|
ENSP00000505877.1:n.*547G>A
|
|
|
ENST00000681278.1:n.1249G>A
|
|
|
|
ENST00000681289.1:n.4887G>A
|
|
|
|
ENST00000681361.1:c.*559G>A
|
ENSP00000506679.1:n.*559G>A
|
|
|
ENST00000681430.1:c.892G>A
|
ENSP00000506301.1:p.Glu298Lys
|
|
|
ENST00000681446.1:c.*474G>A
|
ENSP00000506244.1:n.*474G>A
|
|
|
ENST00000681450.1:c.*563G>A
|
ENSP00000505660.1:n.*563G>A
|
|
|
ENST00000681548.1:c.*478G>A
|
ENSP00000505275.1:n.*478G>A
|
|
|
ENST00000681616.1:c.*551G>A
|
ENSP00000505111.1:n.*551G>A
|
|
|
ENST00000681621.1:c.*476G>A
|
ENSP00000505770.1:n.*476G>A
|
|
|
ENST00000681680.1:n.2987G>A
|
|
|
|
ENST00000681720.1:c.*347G>A
|
ENSP00000505438.1:n.*347G>A
|
|
|
ENST00000681730.1:n.1114G>A
|
|
|
|
ENST00000681790.1:c.634G>A
|
ENSP00000505130.1:p.Glu212Lys
|
|
|
ENST00000681837.1:n.1508G>A
|
|
|
|
ENST00000681913.1:n.3016G>A
|
|
|
|
ENST00000681916.1:c.*660G>A
|
ENSP00000506477.1:n.*660G>A
|
|
|
ENST00000681930.1:n.3016G>A
|
|
|
|
ENST00000370834.9:c.991G>A
|
ENSP00000359871.5:p.Glu331Lys
|
|
|
ENST00000370841.8:c.892G>A
|
ENSP00000359878.4:p.Glu298Lys
|
|
|
ENST00000420607.6:c.904G>A
|
ENSP00000409612.2:p.Glu302Lys
|
|
|
ENST00000481374.1:n.43G>A
|
|
|
|
ENST00000525808.5:c.*478G>A
|
ENSP00000434823.1:n.*478G>A
|
|
|
ENST00000526129.5:c.*676G>A
|
ENSP00000434092.1:n.*676G>A
|
|
|
ENST00000526196.5:c.*660G>A
|
ENSP00000431953.1:n.*660G>A
|
|
|
ENST00000528016.1:c.106G>A
|
ENSP00000434284.1:p.Glu36Lys
|
|
|
ENST00000529059.5:n.801G>A
|
|
|
|
ENST00000532207.5:n.622G>A
|
|
|
|
ENST00000534334.5:c.*476G>A
|
ENSP00000435584.1:n.*476G>A
|
|
|
ENST00000541113.5:c.784G>A
|
ENSP00000442324.1:p.Glu262Lys
|
|
|
NM_000016.5:c.892G>A
|
NP_000007.1:p.Glu298Lys
|
|
|
NM_001127328.2:c.904G>A
|
NP_001120800.1:p.Glu302Lys
|
|
|
NM_001286042.1:c.784G>A
|
NP_001272971.1:p.Glu262Lys
|
|
|
NM_001286043.1:c.991G>A
|
NP_001272972.1:p.Glu331Lys
|
|
|
NM_001286044.1:c.325G>A
|
NP_001272973.1:p.Glu109Lys
|
|
|
NM_000016.6:c.892G>A
MANE Select
|
NP_000007.1:p.Glu298Lys
|
|
|
NM_001127328.3:c.904G>A
|
NP_001120800.1:p.Glu302Lys
|
|
|
NM_001286042.2:c.784G>A
|
NP_001272971.1:p.Glu262Lys
|
|
|
NM_001286043.2:c.991G>A
|
NP_001272972.1:p.Glu331Lys
|
|
|
NM_001286044.2:c.325G>A
|
NP_001272973.1:p.Glu109Lys
|
|
