|
ENST00000370841.9:c.1112A>C
MANE Select
|
ENSP00000359878.5:p.Asp371Ala
|
|
|
ENST00000473018.3:n.3236A>C
|
|
|
|
ENST00000532207.6:n.2123A>C
|
|
|
|
ENST00000541113.6:c.1016A>C
|
ENSP00000442324.2:p.Asp339Ala
|
|
|
ENST00000679509.1:n.2074A>C
|
|
|
|
ENST00000679530.1:c.*880A>C
|
ENSP00000506454.1:n.*880A>C
|
|
|
ENST00000679615.1:n.3127A>C
|
|
|
|
ENST00000679687.1:c.674A>C
|
ENSP00000506598.1:p.Asp225Ala
|
|
|
ENST00000679704.1:c.*878A>C
|
ENSP00000505117.1:n.*878A>C
|
|
|
ENST00000679709.1:c.*1075A>C
|
ENSP00000506623.1:n.*1075A>C
|
|
|
ENST00000679976.1:c.*696A>C
|
ENSP00000505565.1:n.*696A>C
|
|
|
ENST00000680166.1:n.4401A>C
|
|
|
|
ENST00000680315.1:n.995A>C
|
|
|
|
ENST00000680517.1:c.*500A>C
|
ENSP00000505803.1:n.*500A>C
|
|
|
ENST00000680582.1:n.2074A>C
|
|
|
|
ENST00000680613.1:c.*605A>C
|
ENSP00000506114.1:n.*605A>C
|
|
|
ENST00000680662.1:c.*1026A>C
|
ENSP00000505080.1:n.*1026A>C
|
|
|
ENST00000680691.1:c.*775A>C
|
ENSP00000506487.1:n.*775A>C
|
|
|
ENST00000680694.1:c.*700A>C
|
ENSP00000505658.1:n.*700A>C
|
|
|
ENST00000680743.1:c.*901A>C
|
ENSP00000505073.1:n.*901A>C
|
|
|
ENST00000680749.1:c.*397A>C
|
ENSP00000505122.1:n.*397A>C
|
|
|
ENST00000680798.1:c.*587A>C
|
ENSP00000505670.1:n.*587A>C
|
|
|
ENST00000680805.1:c.971A>C
|
ENSP00000505447.1:p.Asp324Ala
|
|
|
ENST00000680844.1:c.*896A>C
|
ENSP00000506541.1:n.*896A>C
|
|
|
ENST00000680948.1:c.*979A>C
|
ENSP00000505441.1:n.*979A>C
|
|
|
ENST00000680964.1:c.*205A>C
|
ENSP00000505961.1:n.*205A>C
|
|
|
ENST00000681037.1:c.*2596A>C
|
ENSP00000506025.1:n.*2596A>C
|
|
|
ENST00000681063.1:c.*381A>C
|
ENSP00000506616.1:n.*381A>C
|
|
|
ENST00000681209.1:c.*767A>C
|
ENSP00000505877.1:n.*767A>C
|
|
|
ENST00000681278.1:n.1814A>C
|
|
|
|
ENST00000681289.1:n.5107A>C
|
|
|
|
ENST00000681361.1:c.*779A>C
|
ENSP00000506679.1:n.*779A>C
|
|
|
ENST00000681430.1:c.*205A>C
|
ENSP00000506301.1:n.*205A>C
|
|
|
ENST00000681446.1:c.*816A>C
|
ENSP00000506244.1:n.*816A>C
|
|
|
ENST00000681450.1:c.*783A>C
|
ENSP00000505660.1:n.*783A>C
|
|
|
ENST00000681548.1:c.*698A>C
|
ENSP00000505275.1:n.*698A>C
|
|
|
ENST00000681616.1:c.*771A>C
|
ENSP00000505111.1:n.*771A>C
|
|
|
ENST00000681621.1:c.*696A>C
|
ENSP00000505770.1:n.*696A>C
|
|
|
ENST00000681680.1:n.3207A>C
|
|
|
|
ENST00000681720.1:c.*567A>C
|
ENSP00000505438.1:n.*567A>C
|
|
|
ENST00000681730.1:n.1334A>C
|
|
|
|
ENST00000681790.1:c.854A>C
|
ENSP00000505130.1:p.Asp285Ala
|
|
|
ENST00000681837.1:n.1728A>C
|
|
|
|
ENST00000681913.1:n.3358A>C
|
|
|
|
ENST00000681916.1:c.*880A>C
|
ENSP00000506477.1:n.*880A>C
|
|
|
ENST00000681930.1:n.3236A>C
|
|
|
|
ENST00000370834.9:c.1211A>C
|
ENSP00000359871.5:p.Asp404Ala
|
|
|
ENST00000370841.8:c.1112A>C
|
ENSP00000359878.4:p.Asp371Ala
|
|
|
ENST00000420607.6:c.1124A>C
|
ENSP00000409612.2:p.Asp375Ala
|
|
|
ENST00000481374.1:n.385A>C
|
|
|
|
ENST00000525808.5:c.*698A>C
|
ENSP00000434823.1:n.*698A>C
|
|
|
ENST00000526129.5:c.*896A>C
|
ENSP00000434092.1:n.*896A>C
|
|
|
ENST00000526196.5:c.*880A>C
|
ENSP00000431953.1:n.*880A>C
|
|
|
ENST00000528016.1:c.160-7889A>C
|
ENSP00000434284.1:n.160-7889A>C
|
|
|
ENST00000529059.5:n.1021A>C
|
|
|
|
ENST00000541113.5:c.1004A>C
|
ENSP00000442324.1:p.Asp335Ala
|
|
|
NM_000016.5:c.1112A>C
|
NP_000007.1:p.Asp371Ala
|
|
|
NM_001127328.2:c.1124A>C
|
NP_001120800.1:p.Asp375Ala
|
|
|
NM_001286042.1:c.1004A>C
|
NP_001272971.1:p.Asp335Ala
|
|
|
NM_001286043.1:c.1211A>C
|
NP_001272972.1:p.Asp404Ala
|
|
|
NM_001286044.1:c.545A>C
|
NP_001272973.1:p.Asp182Ala
|
|
|
NM_000016.6:c.1112A>C
MANE Select
|
NP_000007.1:p.Asp371Ala
|
|
|
NM_001127328.3:c.1124A>C
|
NP_001120800.1:p.Asp375Ala
|
|
|
NM_001286042.2:c.1004A>C
|
NP_001272971.1:p.Asp335Ala
|
|
|
NM_001286043.2:c.1211A>C
|
NP_001272972.1:p.Asp404Ala
|
|
|
NM_001286044.2:c.545A>C
|
NP_001272973.1:p.Asp182Ala
|
|
