|
ENST00000370841.9:c.895G>A
MANE Select
|
ENSP00000359878.5:p.Ala299Thr
|
|
|
ENST00000473018.3:n.3019G>A
|
|
|
|
ENST00000532207.6:n.1784G>A
|
|
|
|
ENST00000541113.6:c.849+937G>A
|
ENSP00000442324.2:n.849+937G>A
|
|
|
ENST00000679509.1:n.1857G>A
|
|
|
|
ENST00000679530.1:c.*663G>A
|
ENSP00000506454.1:n.*663G>A
|
|
|
ENST00000679615.1:n.2910G>A
|
|
|
|
ENST00000679687.1:c.457G>A
|
ENSP00000506598.1:p.Ala153Thr
|
|
|
ENST00000679704.1:c.*661G>A
|
ENSP00000505117.1:n.*661G>A
|
|
|
ENST00000679709.1:c.*858G>A
|
ENSP00000506623.1:n.*858G>A
|
|
|
ENST00000679976.1:c.*479G>A
|
ENSP00000505565.1:n.*479G>A
|
|
|
ENST00000680166.1:n.4184G>A
|
|
|
|
ENST00000680315.1:n.778G>A
|
|
|
|
ENST00000680517.1:c.*283G>A
|
ENSP00000505803.1:n.*283G>A
|
|
|
ENST00000680582.1:n.1857G>A
|
|
|
|
ENST00000680613.1:c.*266G>A
|
ENSP00000506114.1:n.*266G>A
|
|
|
ENST00000680662.1:c.*809G>A
|
ENSP00000505080.1:n.*809G>A
|
|
|
ENST00000680691.1:c.*558G>A
|
ENSP00000506487.1:n.*558G>A
|
|
|
ENST00000680694.1:c.*483G>A
|
ENSP00000505658.1:n.*483G>A
|
|
|
ENST00000680743.1:c.*562G>A
|
ENSP00000505073.1:n.*562G>A
|
|
|
ENST00000680749.1:c.*180G>A
|
ENSP00000505122.1:n.*180G>A
|
|
|
ENST00000680798.1:c.*370G>A
|
ENSP00000505670.1:n.*370G>A
|
|
|
ENST00000680805.1:c.754G>A
|
ENSP00000505447.1:p.Ala252Thr
|
|
|
ENST00000680844.1:c.*679G>A
|
ENSP00000506541.1:n.*679G>A
|
|
|
ENST00000680948.1:c.*762G>A
|
ENSP00000505441.1:n.*762G>A
|
|
|
ENST00000680964.1:c.895G>A
|
ENSP00000505961.1:p.Ala299Thr
|
|
|
ENST00000681037.1:c.*2379G>A
|
ENSP00000506025.1:n.*2379G>A
|
|
|
ENST00000681063.1:c.*42G>A
|
ENSP00000506616.1:n.*42G>A
|
|
|
ENST00000681209.1:c.*550G>A
|
ENSP00000505877.1:n.*550G>A
|
|
|
ENST00000681278.1:n.1252G>A
|
|
|
|
ENST00000681289.1:n.4890G>A
|
|
|
|
ENST00000681361.1:c.*562G>A
|
ENSP00000506679.1:n.*562G>A
|
|
|
ENST00000681430.1:c.895G>A
|
ENSP00000506301.1:p.Ala299Thr
|
|
|
ENST00000681446.1:c.*477G>A
|
ENSP00000506244.1:n.*477G>A
|
|
|
ENST00000681450.1:c.*566G>A
|
ENSP00000505660.1:n.*566G>A
|
|
|
ENST00000681548.1:c.*481G>A
|
ENSP00000505275.1:n.*481G>A
|
|
|
ENST00000681616.1:c.*554G>A
|
ENSP00000505111.1:n.*554G>A
|
|
|
ENST00000681621.1:c.*479G>A
|
ENSP00000505770.1:n.*479G>A
|
|
|
ENST00000681680.1:n.2990G>A
|
|
|
|
ENST00000681720.1:c.*350G>A
|
ENSP00000505438.1:n.*350G>A
|
|
|
ENST00000681730.1:n.1117G>A
|
|
|
|
ENST00000681790.1:c.637G>A
|
ENSP00000505130.1:p.Ala213Thr
|
|
|
ENST00000681837.1:n.1511G>A
|
|
|
|
ENST00000681913.1:n.3019G>A
|
|
|
|
ENST00000681916.1:c.*663G>A
|
ENSP00000506477.1:n.*663G>A
|
|
|
ENST00000681930.1:n.3019G>A
|
|
|
|
ENST00000370834.9:c.994G>A
|
ENSP00000359871.5:p.Ala332Thr
|
|
|
ENST00000370841.8:c.895G>A
|
ENSP00000359878.4:p.Ala299Thr
|
|
|
ENST00000420607.6:c.907G>A
|
ENSP00000409612.2:p.Ala303Thr
|
|
|
ENST00000481374.1:n.46G>A
|
|
|
|
ENST00000525808.5:c.*481G>A
|
ENSP00000434823.1:n.*481G>A
|
|
|
ENST00000526129.5:c.*679G>A
|
ENSP00000434092.1:n.*679G>A
|
|
|
ENST00000526196.5:c.*663G>A
|
ENSP00000431953.1:n.*663G>A
|
|
|
ENST00000528016.1:c.109G>A
|
ENSP00000434284.1:p.Ala37Thr
|
|
|
ENST00000529059.5:n.804G>A
|
|
|
|
ENST00000532207.5:n.625G>A
|
|
|
|
ENST00000534334.5:c.*479G>A
|
ENSP00000435584.1:n.*479G>A
|
|
|
ENST00000541113.5:c.787G>A
|
ENSP00000442324.1:p.Ala263Thr
|
|
|
NM_000016.5:c.895G>A
|
NP_000007.1:p.Ala299Thr
|
|
|
NM_001127328.2:c.907G>A
|
NP_001120800.1:p.Ala303Thr
|
|
|
NM_001286042.1:c.787G>A
|
NP_001272971.1:p.Ala263Thr
|
|
|
NM_001286043.1:c.994G>A
|
NP_001272972.1:p.Ala332Thr
|
|
|
NM_001286044.1:c.328G>A
|
NP_001272973.1:p.Ala110Thr
|
|
|
NM_000016.6:c.895G>A
MANE Select
|
NP_000007.1:p.Ala299Thr
|
|
|
NM_001127328.3:c.907G>A
|
NP_001120800.1:p.Ala303Thr
|
|
|
NM_001286042.2:c.787G>A
|
NP_001272971.1:p.Ala263Thr
|
|
|
NM_001286043.2:c.994G>A
|
NP_001272972.1:p.Ala332Thr
|
|
|
NM_001286044.2:c.328G>A
|
NP_001272973.1:p.Ala110Thr
|
|
