|
ENST00000370841.9:c.799G>C
MANE Select
|
ENSP00000359878.5:p.Gly267Arg
|
|
|
ENST00000473018.3:n.2923G>C
|
|
|
|
ENST00000532207.6:n.1688G>C
|
|
|
|
ENST00000541113.6:c.799G>C
|
ENSP00000442324.2:p.Gly267Arg
|
|
|
ENST00000679509.1:n.1761G>C
|
|
|
|
ENST00000679530.1:c.*567G>C
|
ENSP00000506454.1:n.*567G>C
|
|
|
ENST00000679615.1:n.2814G>C
|
|
|
|
ENST00000679687.1:c.361G>C
|
ENSP00000506598.1:p.Gly121Arg
|
|
|
ENST00000679704.1:c.*565G>C
|
ENSP00000505117.1:n.*565G>C
|
|
|
ENST00000679709.1:c.*762G>C
|
ENSP00000506623.1:n.*762G>C
|
|
|
ENST00000679976.1:c.*383G>C
|
ENSP00000505565.1:n.*383G>C
|
|
|
ENST00000680166.1:n.4088G>C
|
|
|
|
ENST00000680517.1:c.*187G>C
|
ENSP00000505803.1:n.*187G>C
|
|
|
ENST00000680582.1:n.1761G>C
|
|
|
|
ENST00000680613.1:c.*170G>C
|
ENSP00000506114.1:n.*170G>C
|
|
|
ENST00000680662.1:c.*713G>C
|
ENSP00000505080.1:n.*713G>C
|
|
|
ENST00000680691.1:c.*462G>C
|
ENSP00000506487.1:n.*462G>C
|
|
|
ENST00000680694.1:c.*387G>C
|
ENSP00000505658.1:n.*387G>C
|
|
|
ENST00000680743.1:c.*466G>C
|
ENSP00000505073.1:n.*466G>C
|
|
|
ENST00000680749.1:c.*84G>C
|
ENSP00000505122.1:n.*84G>C
|
|
|
ENST00000680798.1:c.*274G>C
|
ENSP00000505670.1:n.*274G>C
|
|
|
ENST00000680805.1:c.709-942G>C
|
ENSP00000505447.1:n.709-942G>C
|
|
|
ENST00000680844.1:c.*583G>C
|
ENSP00000506541.1:n.*583G>C
|
|
|
ENST00000680948.1:c.*666G>C
|
ENSP00000505441.1:n.*666G>C
|
|
|
ENST00000680964.1:c.799G>C
|
ENSP00000505961.1:p.Gly267Arg
|
|
|
ENST00000681037.1:c.*2283G>C
|
ENSP00000506025.1:n.*2283G>C
|
|
|
ENST00000681063.1:c.600-942G>C
|
ENSP00000506616.1:n.600-942G>C
|
|
|
ENST00000681209.1:c.*454G>C
|
ENSP00000505877.1:n.*454G>C
|
|
|
ENST00000681278.1:n.1156G>C
|
|
|
|
ENST00000681289.1:n.4794G>C
|
|
|
|
ENST00000681361.1:c.*466G>C
|
ENSP00000506679.1:n.*466G>C
|
|
|
ENST00000681430.1:c.799G>C
|
ENSP00000506301.1:p.Gly267Arg
|
|
|
ENST00000681446.1:c.*381G>C
|
ENSP00000506244.1:n.*381G>C
|
|
|
ENST00000681450.1:c.*470G>C
|
ENSP00000505660.1:n.*470G>C
|
|
|
ENST00000681548.1:c.*385G>C
|
ENSP00000505275.1:n.*385G>C
|
|
|
ENST00000681616.1:c.*458G>C
|
ENSP00000505111.1:n.*458G>C
|
|
|
ENST00000681621.1:c.*383G>C
|
ENSP00000505770.1:n.*383G>C
|
|
|
ENST00000681680.1:n.2894G>C
|
|
|
|
ENST00000681720.1:c.*254G>C
|
ENSP00000505438.1:n.*254G>C
|
|
|
ENST00000681730.1:n.1021G>C
|
|
|
|
ENST00000681790.1:c.541G>C
|
ENSP00000505130.1:p.Gly181Arg
|
|
|
ENST00000681837.1:n.1415G>C
|
|
|
|
ENST00000681913.1:n.2923G>C
|
|
|
|
ENST00000681916.1:c.*567G>C
|
ENSP00000506477.1:n.*567G>C
|
|
|
ENST00000681930.1:n.2923G>C
|
|
|
|
ENST00000370834.9:c.898G>C
|
ENSP00000359871.5:p.Gly300Arg
|
|
|
ENST00000370841.8:c.799G>C
|
ENSP00000359878.4:p.Gly267Arg
|
|
|
ENST00000420607.6:c.811G>C
|
ENSP00000409612.2:p.Gly271Arg
|
|
|
ENST00000525808.5:c.*385G>C
|
ENSP00000434823.1:n.*385G>C
|
|
|
ENST00000526129.5:c.*583G>C
|
ENSP00000434092.1:n.*583G>C
|
|
|
ENST00000526196.5:c.*567G>C
|
ENSP00000431953.1:n.*567G>C
|
|
|
ENST00000526930.1:n.572G>C
|
|
|
|
ENST00000528016.1:c.13G>C
|
ENSP00000434284.1:p.Gly5Arg
|
|
|
ENST00000529059.5:n.708G>C
|
|
|
|
ENST00000530953.6:c.*296G>C
|
ENSP00000431372.1:n.*296G>C
|
|
|
ENST00000532207.5:n.529G>C
|
|
|
|
ENST00000532509.5:c.*563G>C
|
ENSP00000432522.1:n.*563G>C
|
|
|
ENST00000534334.5:c.*383G>C
|
ENSP00000435584.1:n.*383G>C
|
|
|
ENST00000541113.5:c.691G>C
|
ENSP00000442324.1:p.Gly231Arg
|
|
|
NM_000016.5:c.799G>C
|
NP_000007.1:p.Gly267Arg
|
|
|
NM_001127328.2:c.811G>C
|
NP_001120800.1:p.Gly271Arg
|
|
|
NM_001286042.1:c.691G>C
|
NP_001272971.1:p.Gly231Arg
|
|
|
NM_001286043.1:c.898G>C
|
NP_001272972.1:p.Gly300Arg
|
|
|
NM_001286044.1:c.232G>C
|
NP_001272973.1:p.Gly78Arg
|
|
|
NM_000016.6:c.799G>C
MANE Select
|
NP_000007.1:p.Gly267Arg
|
|
|
NM_001127328.3:c.811G>C
|
NP_001120800.1:p.Gly271Arg
|
|
|
NM_001286042.2:c.691G>C
|
NP_001272971.1:p.Gly231Arg
|
|
|
NM_001286043.2:c.898G>C
|
NP_001272972.1:p.Gly300Arg
|
|
|
NM_001286044.2:c.232G>C
|
NP_001272973.1:p.Gly78Arg
|
|
