|
ENST00000370841.9:c.1133G>C
MANE Select
|
ENSP00000359878.5:p.Gly378Ala
|
|
|
ENST00000473018.3:n.3257G>C
|
|
|
|
ENST00000532207.6:n.2144G>C
|
|
|
|
ENST00000541113.6:c.1037G>C
|
ENSP00000442324.2:p.Gly346Ala
|
|
|
ENST00000679509.1:n.2095G>C
|
|
|
|
ENST00000679530.1:c.*901G>C
|
ENSP00000506454.1:n.*901G>C
|
|
|
ENST00000679615.1:n.3148G>C
|
|
|
|
ENST00000679687.1:c.695G>C
|
ENSP00000506598.1:p.Gly232Ala
|
|
|
ENST00000679704.1:c.*899G>C
|
ENSP00000505117.1:n.*899G>C
|
|
|
ENST00000679709.1:c.*1096G>C
|
ENSP00000506623.1:n.*1096G>C
|
|
|
ENST00000679976.1:c.*717G>C
|
ENSP00000505565.1:n.*717G>C
|
|
|
ENST00000680166.1:n.4422G>C
|
|
|
|
ENST00000680315.1:n.1016G>C
|
|
|
|
ENST00000680517.1:c.*521G>C
|
ENSP00000505803.1:n.*521G>C
|
|
|
ENST00000680582.1:n.2095G>C
|
|
|
|
ENST00000680613.1:c.*626G>C
|
ENSP00000506114.1:n.*626G>C
|
|
|
ENST00000680662.1:c.*1047G>C
|
ENSP00000505080.1:n.*1047G>C
|
|
|
ENST00000680691.1:c.*796G>C
|
ENSP00000506487.1:n.*796G>C
|
|
|
ENST00000680694.1:c.*721G>C
|
ENSP00000505658.1:n.*721G>C
|
|
|
ENST00000680743.1:c.*922G>C
|
ENSP00000505073.1:n.*922G>C
|
|
|
ENST00000680749.1:c.*418G>C
|
ENSP00000505122.1:n.*418G>C
|
|
|
ENST00000680798.1:c.*608G>C
|
ENSP00000505670.1:n.*608G>C
|
|
|
ENST00000680805.1:c.992G>C
|
ENSP00000505447.1:p.Gly331Ala
|
|
|
ENST00000680844.1:c.*917G>C
|
ENSP00000506541.1:n.*917G>C
|
|
|
ENST00000680948.1:c.*1000G>C
|
ENSP00000505441.1:n.*1000G>C
|
|
|
ENST00000680964.1:c.*226G>C
|
ENSP00000505961.1:n.*226G>C
|
|
|
ENST00000681037.1:c.*2617G>C
|
ENSP00000506025.1:n.*2617G>C
|
|
|
ENST00000681063.1:c.*402G>C
|
ENSP00000506616.1:n.*402G>C
|
|
|
ENST00000681209.1:c.*788G>C
|
ENSP00000505877.1:n.*788G>C
|
|
|
ENST00000681278.1:n.1835G>C
|
|
|
|
ENST00000681289.1:n.5128G>C
|
|
|
|
ENST00000681361.1:c.*800G>C
|
ENSP00000506679.1:n.*800G>C
|
|
|
ENST00000681430.1:c.*226G>C
|
ENSP00000506301.1:n.*226G>C
|
|
|
ENST00000681446.1:c.*837G>C
|
ENSP00000506244.1:n.*837G>C
|
|
|
ENST00000681450.1:c.*804G>C
|
ENSP00000505660.1:n.*804G>C
|
|
|
ENST00000681548.1:c.*719G>C
|
ENSP00000505275.1:n.*719G>C
|
|
|
ENST00000681616.1:c.*792G>C
|
ENSP00000505111.1:n.*792G>C
|
|
|
ENST00000681621.1:c.*717G>C
|
ENSP00000505770.1:n.*717G>C
|
|
|
ENST00000681680.1:n.3228G>C
|
|
|
|
ENST00000681720.1:c.*588G>C
|
ENSP00000505438.1:n.*588G>C
|
|
|
ENST00000681730.1:n.1355G>C
|
|
|
|
ENST00000681790.1:c.875G>C
|
ENSP00000505130.1:p.Gly292Ala
|
|
|
ENST00000681837.1:n.1749G>C
|
|
|
|
ENST00000681913.1:n.3379G>C
|
|
|
|
ENST00000681916.1:c.*901G>C
|
ENSP00000506477.1:n.*901G>C
|
|
|
ENST00000681930.1:n.3257G>C
|
|
|
|
ENST00000370834.9:c.1232G>C
|
ENSP00000359871.5:p.Gly411Ala
|
|
|
ENST00000370841.8:c.1133G>C
|
ENSP00000359878.4:p.Gly378Ala
|
|
|
ENST00000420607.6:c.1145G>C
|
ENSP00000409612.2:p.Gly382Ala
|
|
|
ENST00000481374.1:n.406G>C
|
|
|
|
ENST00000525808.5:c.*719G>C
|
ENSP00000434823.1:n.*719G>C
|
|
|
ENST00000526129.5:c.*917G>C
|
ENSP00000434092.1:n.*917G>C
|
|
|
ENST00000526196.5:c.*901G>C
|
ENSP00000431953.1:n.*901G>C
|
|
|
ENST00000528016.1:c.160-7868G>C
|
ENSP00000434284.1:n.160-7868G>C
|
|
|
ENST00000529059.5:n.1042G>C
|
|
|
|
ENST00000541113.5:c.1025G>C
|
ENSP00000442324.1:p.Gly342Ala
|
|
|
NM_000016.5:c.1133G>C
|
NP_000007.1:p.Gly378Ala
|
|
|
NM_001127328.2:c.1145G>C
|
NP_001120800.1:p.Gly382Ala
|
|
|
NM_001286042.1:c.1025G>C
|
NP_001272971.1:p.Gly342Ala
|
|
|
NM_001286043.1:c.1232G>C
|
NP_001272972.1:p.Gly411Ala
|
|
|
NM_001286044.1:c.566G>C
|
NP_001272973.1:p.Gly189Ala
|
|
|
NM_000016.6:c.1133G>C
MANE Select
|
NP_000007.1:p.Gly378Ala
|
|
|
NM_001127328.3:c.1145G>C
|
NP_001120800.1:p.Gly382Ala
|
|
|
NM_001286042.2:c.1025G>C
|
NP_001272971.1:p.Gly342Ala
|
|
|
NM_001286043.2:c.1232G>C
|
NP_001272972.1:p.Gly411Ala
|
|
|
NM_001286044.2:c.566G>C
|
NP_001272973.1:p.Gly189Ala
|
|
