|
ENST00000370841.9:c.1001G>C
MANE Select
|
ENSP00000359878.5:p.Arg334Thr
|
|
|
ENST00000473018.3:n.3125G>C
|
|
|
|
ENST00000532207.6:n.2012G>C
|
|
|
|
ENST00000541113.6:c.905G>C
|
ENSP00000442324.2:p.Arg302Thr
|
|
|
ENST00000679509.1:n.1963G>C
|
|
|
|
ENST00000679530.1:c.*769G>C
|
ENSP00000506454.1:n.*769G>C
|
|
|
ENST00000679615.1:n.3016G>C
|
|
|
|
ENST00000679687.1:c.563G>C
|
ENSP00000506598.1:p.Arg188Thr
|
|
|
ENST00000679704.1:c.*767G>C
|
ENSP00000505117.1:n.*767G>C
|
|
|
ENST00000679709.1:c.*964G>C
|
ENSP00000506623.1:n.*964G>C
|
|
|
ENST00000679976.1:c.*585G>C
|
ENSP00000505565.1:n.*585G>C
|
|
|
ENST00000680166.1:n.4290G>C
|
|
|
|
ENST00000680315.1:n.884G>C
|
|
|
|
ENST00000680517.1:c.*389G>C
|
ENSP00000505803.1:n.*389G>C
|
|
|
ENST00000680582.1:n.1963G>C
|
|
|
|
ENST00000680613.1:c.*494G>C
|
ENSP00000506114.1:n.*494G>C
|
|
|
ENST00000680662.1:c.*915G>C
|
ENSP00000505080.1:n.*915G>C
|
|
|
ENST00000680691.1:c.*664G>C
|
ENSP00000506487.1:n.*664G>C
|
|
|
ENST00000680694.1:c.*589G>C
|
ENSP00000505658.1:n.*589G>C
|
|
|
ENST00000680743.1:c.*790G>C
|
ENSP00000505073.1:n.*790G>C
|
|
|
ENST00000680749.1:c.*286G>C
|
ENSP00000505122.1:n.*286G>C
|
|
|
ENST00000680798.1:c.*476G>C
|
ENSP00000505670.1:n.*476G>C
|
|
|
ENST00000680805.1:c.860G>C
|
ENSP00000505447.1:p.Arg287Thr
|
|
|
ENST00000680844.1:c.*785G>C
|
ENSP00000506541.1:n.*785G>C
|
|
|
ENST00000680948.1:c.*868G>C
|
ENSP00000505441.1:n.*868G>C
|
|
|
ENST00000680964.1:c.*94G>C
|
ENSP00000505961.1:n.*94G>C
|
|
|
ENST00000681037.1:c.*2485G>C
|
ENSP00000506025.1:n.*2485G>C
|
|
|
ENST00000681063.1:c.*270G>C
|
ENSP00000506616.1:n.*270G>C
|
|
|
ENST00000681209.1:c.*656G>C
|
ENSP00000505877.1:n.*656G>C
|
|
|
ENST00000681278.1:n.1703G>C
|
|
|
|
ENST00000681289.1:n.4996G>C
|
|
|
|
ENST00000681361.1:c.*668G>C
|
ENSP00000506679.1:n.*668G>C
|
|
|
ENST00000681430.1:c.*94G>C
|
ENSP00000506301.1:n.*94G>C
|
|
|
ENST00000681446.1:c.*705G>C
|
ENSP00000506244.1:n.*705G>C
|
|
|
ENST00000681450.1:c.*672G>C
|
ENSP00000505660.1:n.*672G>C
|
|
|
ENST00000681548.1:c.*587G>C
|
ENSP00000505275.1:n.*587G>C
|
|
|
ENST00000681616.1:c.*660G>C
|
ENSP00000505111.1:n.*660G>C
|
|
|
ENST00000681621.1:c.*585G>C
|
ENSP00000505770.1:n.*585G>C
|
|
|
ENST00000681680.1:n.3096G>C
|
|
|
|
ENST00000681720.1:c.*456G>C
|
ENSP00000505438.1:n.*456G>C
|
|
|
ENST00000681730.1:n.1223G>C
|
|
|
|
ENST00000681790.1:c.743G>C
|
ENSP00000505130.1:p.Arg248Thr
|
|
|
ENST00000681837.1:n.1617G>C
|
|
|
|
ENST00000681913.1:n.3247G>C
|
|
|
|
ENST00000681916.1:c.*769G>C
|
ENSP00000506477.1:n.*769G>C
|
|
|
ENST00000681930.1:n.3125G>C
|
|
|
|
ENST00000370834.9:c.1100G>C
|
ENSP00000359871.5:p.Arg367Thr
|
|
|
ENST00000370841.8:c.1001G>C
|
ENSP00000359878.4:p.Arg334Thr
|
|
|
ENST00000420607.6:c.1013G>C
|
ENSP00000409612.2:p.Arg338Thr
|
|
|
ENST00000481374.1:n.274G>C
|
|
|
|
ENST00000525808.5:c.*587G>C
|
ENSP00000434823.1:n.*587G>C
|
|
|
ENST00000526129.5:c.*785G>C
|
ENSP00000434092.1:n.*785G>C
|
|
|
ENST00000526196.5:c.*769G>C
|
ENSP00000431953.1:n.*769G>C
|
|
|
ENST00000528016.1:c.160-8000G>C
|
ENSP00000434284.1:n.160-8000G>C
|
|
|
ENST00000529059.5:n.910G>C
|
|
|
|
ENST00000532207.5:n.731G>C
|
|
|
|
ENST00000534334.5:c.*742G>C
|
ENSP00000435584.1:n.*742G>C
|
|
|
ENST00000541113.5:c.893G>C
|
ENSP00000442324.1:p.Arg298Thr
|
|
|
NM_000016.5:c.1001G>C
|
NP_000007.1:p.Arg334Thr
|
|
|
NM_001127328.2:c.1013G>C
|
NP_001120800.1:p.Arg338Thr
|
|
|
NM_001286042.1:c.893G>C
|
NP_001272971.1:p.Arg298Thr
|
|
|
NM_001286043.1:c.1100G>C
|
NP_001272972.1:p.Arg367Thr
|
|
|
NM_001286044.1:c.434G>C
|
NP_001272973.1:p.Arg145Thr
|
|
|
NM_000016.6:c.1001G>C
MANE Select
|
NP_000007.1:p.Arg334Thr
|
|
|
NM_001127328.3:c.1013G>C
|
NP_001120800.1:p.Arg338Thr
|
|
|
NM_001286042.2:c.893G>C
|
NP_001272971.1:p.Arg298Thr
|
|
|
NM_001286043.2:c.1100G>C
|
NP_001272972.1:p.Arg367Thr
|
|
|
NM_001286044.2:c.434G>C
|
NP_001272973.1:p.Arg145Thr
|
|
