|
ENST00000370841.9:c.1189T>C
MANE Select
|
ENSP00000359878.5:p.Tyr397His
|
|
|
ENST00000473018.3:n.3313T>C
|
|
|
|
ENST00000532207.6:n.2200T>C
|
|
|
|
ENST00000541113.6:c.1093T>C
|
ENSP00000442324.2:p.Tyr365His
|
|
|
ENST00000679509.1:n.2151T>C
|
|
|
|
ENST00000679530.1:c.*957T>C
|
ENSP00000506454.1:n.*957T>C
|
|
|
ENST00000679615.1:n.3204T>C
|
|
|
|
ENST00000679687.1:c.751T>C
|
ENSP00000506598.1:p.Tyr251His
|
|
|
ENST00000679704.1:c.*955T>C
|
ENSP00000505117.1:n.*955T>C
|
|
|
ENST00000679709.1:c.*1152T>C
|
ENSP00000506623.1:n.*1152T>C
|
|
|
ENST00000679976.1:c.*773T>C
|
ENSP00000505565.1:n.*773T>C
|
|
|
ENST00000680166.1:n.4478T>C
|
|
|
|
ENST00000680315.1:n.1072T>C
|
|
|
|
ENST00000680517.1:c.*577T>C
|
ENSP00000505803.1:n.*577T>C
|
|
|
ENST00000680582.1:n.2151T>C
|
|
|
|
ENST00000680613.1:c.*682T>C
|
ENSP00000506114.1:n.*682T>C
|
|
|
ENST00000680662.1:c.*1103T>C
|
ENSP00000505080.1:n.*1103T>C
|
|
|
ENST00000680691.1:c.*852T>C
|
ENSP00000506487.1:n.*852T>C
|
|
|
ENST00000680694.1:c.*777T>C
|
ENSP00000505658.1:n.*777T>C
|
|
|
ENST00000680743.1:c.*978T>C
|
ENSP00000505073.1:n.*978T>C
|
|
|
ENST00000680749.1:c.*474T>C
|
ENSP00000505122.1:n.*474T>C
|
|
|
ENST00000680798.1:c.*664T>C
|
ENSP00000505670.1:n.*664T>C
|
|
|
ENST00000680805.1:c.1048T>C
|
ENSP00000505447.1:p.Tyr350His
|
|
|
ENST00000680844.1:c.*973T>C
|
ENSP00000506541.1:n.*973T>C
|
|
|
ENST00000680948.1:c.*1056T>C
|
ENSP00000505441.1:n.*1056T>C
|
|
|
ENST00000680964.1:c.*282T>C
|
ENSP00000505961.1:n.*282T>C
|
|
|
ENST00000681037.1:c.*2673T>C
|
ENSP00000506025.1:n.*2673T>C
|
|
|
ENST00000681063.1:c.*458T>C
|
ENSP00000506616.1:n.*458T>C
|
|
|
ENST00000681209.1:c.*844T>C
|
ENSP00000505877.1:n.*844T>C
|
|
|
ENST00000681278.1:n.1891T>C
|
|
|
|
ENST00000681289.1:n.5184T>C
|
|
|
|
ENST00000681361.1:c.*856T>C
|
ENSP00000506679.1:n.*856T>C
|
|
|
ENST00000681430.1:c.*282T>C
|
ENSP00000506301.1:n.*282T>C
|
|
|
ENST00000681446.1:c.*893T>C
|
ENSP00000506244.1:n.*893T>C
|
|
|
ENST00000681450.1:c.*860T>C
|
ENSP00000505660.1:n.*860T>C
|
|
|
ENST00000681548.1:c.*775T>C
|
ENSP00000505275.1:n.*775T>C
|
|
|
ENST00000681616.1:c.*848T>C
|
ENSP00000505111.1:n.*848T>C
|
|
|
ENST00000681621.1:c.*773T>C
|
ENSP00000505770.1:n.*773T>C
|
|
|
ENST00000681680.1:n.3284T>C
|
|
|
|
ENST00000681720.1:c.*644T>C
|
ENSP00000505438.1:n.*644T>C
|
|
|
ENST00000681730.1:n.1411T>C
|
|
|
|
ENST00000681790.1:c.931T>C
|
ENSP00000505130.1:p.Tyr311His
|
|
|
ENST00000681837.1:n.1805T>C
|
|
|
|
ENST00000681913.1:n.3435T>C
|
|
|
|
ENST00000681916.1:c.*957T>C
|
ENSP00000506477.1:n.*957T>C
|
|
|
ENST00000681930.1:n.3313T>C
|
|
|
|
ENST00000370834.9:c.1288T>C
|
ENSP00000359871.5:p.Tyr430His
|
|
|
ENST00000370841.8:c.1189T>C
|
ENSP00000359878.4:p.Tyr397His
|
|
|
ENST00000420607.6:c.1201T>C
|
ENSP00000409612.2:p.Tyr401His
|
|
|
ENST00000481374.1:n.462T>C
|
|
|
|
ENST00000525808.5:c.*775T>C
|
ENSP00000434823.1:n.*775T>C
|
|
|
ENST00000526129.5:c.*973T>C
|
ENSP00000434092.1:n.*973T>C
|
|
|
ENST00000526196.5:c.*957T>C
|
ENSP00000431953.1:n.*957T>C
|
|
|
ENST00000528016.1:c.160-7812T>C
|
ENSP00000434284.1:n.160-7812T>C
|
|
|
ENST00000529059.5:n.1098T>C
|
|
|
|
ENST00000541113.5:c.1081T>C
|
ENSP00000442324.1:p.Tyr361His
|
|
|
NM_000016.5:c.1189T>C
|
NP_000007.1:p.Tyr397His
|
|
|
NM_001127328.2:c.1201T>C
|
NP_001120800.1:p.Tyr401His
|
|
|
NM_001286042.1:c.1081T>C
|
NP_001272971.1:p.Tyr361His
|
|
|
NM_001286043.1:c.1288T>C
|
NP_001272972.1:p.Tyr430His
|
|
|
NM_001286044.1:c.622T>C
|
NP_001272973.1:p.Tyr208His
|
|
|
NM_000016.6:c.1189T>C
MANE Select
|
NP_000007.1:p.Tyr397His
|
|
|
NM_001127328.3:c.1201T>C
|
NP_001120800.1:p.Tyr401His
|
|
|
NM_001286042.2:c.1081T>C
|
NP_001272971.1:p.Tyr361His
|
|
|
NM_001286043.2:c.1288T>C
|
NP_001272972.1:p.Tyr430His
|
|
|
NM_001286044.2:c.622T>C
|
NP_001272973.1:p.Tyr208His
|
|
