|
ENST00000370841.9:c.872T>C
MANE Select
|
ENSP00000359878.5:p.Leu291Ser
|
|
|
ENST00000473018.3:n.2996T>C
|
|
|
|
ENST00000532207.6:n.1761T>C
|
|
|
|
ENST00000541113.6:c.849+914T>C
|
ENSP00000442324.2:n.849+914T>C
|
|
|
ENST00000679509.1:n.1834T>C
|
|
|
|
ENST00000679530.1:c.*640T>C
|
ENSP00000506454.1:n.*640T>C
|
|
|
ENST00000679615.1:n.2887T>C
|
|
|
|
ENST00000679687.1:c.434T>C
|
ENSP00000506598.1:p.Leu145Ser
|
|
|
ENST00000679704.1:c.*638T>C
|
ENSP00000505117.1:n.*638T>C
|
|
|
ENST00000679709.1:c.*835T>C
|
ENSP00000506623.1:n.*835T>C
|
|
|
ENST00000679976.1:c.*456T>C
|
ENSP00000505565.1:n.*456T>C
|
|
|
ENST00000680166.1:n.4161T>C
|
|
|
|
ENST00000680315.1:n.755T>C
|
|
|
|
ENST00000680517.1:c.*260T>C
|
ENSP00000505803.1:n.*260T>C
|
|
|
ENST00000680582.1:n.1834T>C
|
|
|
|
ENST00000680613.1:c.*243T>C
|
ENSP00000506114.1:n.*243T>C
|
|
|
ENST00000680662.1:c.*786T>C
|
ENSP00000505080.1:n.*786T>C
|
|
|
ENST00000680691.1:c.*535T>C
|
ENSP00000506487.1:n.*535T>C
|
|
|
ENST00000680694.1:c.*460T>C
|
ENSP00000505658.1:n.*460T>C
|
|
|
ENST00000680743.1:c.*539T>C
|
ENSP00000505073.1:n.*539T>C
|
|
|
ENST00000680749.1:c.*157T>C
|
ENSP00000505122.1:n.*157T>C
|
|
|
ENST00000680798.1:c.*347T>C
|
ENSP00000505670.1:n.*347T>C
|
|
|
ENST00000680805.1:c.731T>C
|
ENSP00000505447.1:p.Leu244Ser
|
|
|
ENST00000680844.1:c.*656T>C
|
ENSP00000506541.1:n.*656T>C
|
|
|
ENST00000680948.1:c.*739T>C
|
ENSP00000505441.1:n.*739T>C
|
|
|
ENST00000680964.1:c.872T>C
|
ENSP00000505961.1:p.Leu291Ser
|
|
|
ENST00000681037.1:c.*2356T>C
|
ENSP00000506025.1:n.*2356T>C
|
|
|
ENST00000681063.1:c.*19T>C
|
ENSP00000506616.1:n.*19T>C
|
|
|
ENST00000681209.1:c.*527T>C
|
ENSP00000505877.1:n.*527T>C
|
|
|
ENST00000681278.1:n.1229T>C
|
|
|
|
ENST00000681289.1:n.4867T>C
|
|
|
|
ENST00000681361.1:c.*539T>C
|
ENSP00000506679.1:n.*539T>C
|
|
|
ENST00000681430.1:c.872T>C
|
ENSP00000506301.1:p.Leu291Ser
|
|
|
ENST00000681446.1:c.*454T>C
|
ENSP00000506244.1:n.*454T>C
|
|
|
ENST00000681450.1:c.*543T>C
|
ENSP00000505660.1:n.*543T>C
|
|
|
ENST00000681548.1:c.*458T>C
|
ENSP00000505275.1:n.*458T>C
|
|
|
ENST00000681616.1:c.*531T>C
|
ENSP00000505111.1:n.*531T>C
|
|
|
ENST00000681621.1:c.*456T>C
|
ENSP00000505770.1:n.*456T>C
|
|
|
ENST00000681680.1:n.2967T>C
|
|
|
|
ENST00000681720.1:c.*327T>C
|
ENSP00000505438.1:n.*327T>C
|
|
|
ENST00000681730.1:n.1094T>C
|
|
|
|
ENST00000681790.1:c.614T>C
|
ENSP00000505130.1:p.Leu205Ser
|
|
|
ENST00000681837.1:n.1488T>C
|
|
|
|
ENST00000681913.1:n.2996T>C
|
|
|
|
ENST00000681916.1:c.*640T>C
|
ENSP00000506477.1:n.*640T>C
|
|
|
ENST00000681930.1:n.2996T>C
|
|
|
|
ENST00000370834.9:c.971T>C
|
ENSP00000359871.5:p.Leu324Ser
|
|
|
ENST00000370841.8:c.872T>C
|
ENSP00000359878.4:p.Leu291Ser
|
|
|
ENST00000420607.6:c.884T>C
|
ENSP00000409612.2:p.Leu295Ser
|
|
|
ENST00000481374.1:n.23T>C
|
|
|
|
ENST00000525808.5:c.*458T>C
|
ENSP00000434823.1:n.*458T>C
|
|
|
ENST00000526129.5:c.*656T>C
|
ENSP00000434092.1:n.*656T>C
|
|
|
ENST00000526196.5:c.*640T>C
|
ENSP00000431953.1:n.*640T>C
|
|
|
ENST00000528016.1:c.86T>C
|
ENSP00000434284.1:p.Leu29Ser
|
|
|
ENST00000529059.5:n.781T>C
|
|
|
|
ENST00000532207.5:n.602T>C
|
|
|
|
ENST00000534334.5:c.*456T>C
|
ENSP00000435584.1:n.*456T>C
|
|
|
ENST00000541113.5:c.764T>C
|
ENSP00000442324.1:p.Leu255Ser
|
|
|
NM_000016.5:c.872T>C
|
NP_000007.1:p.Leu291Ser
|
|
|
NM_001127328.2:c.884T>C
|
NP_001120800.1:p.Leu295Ser
|
|
|
NM_001286042.1:c.764T>C
|
NP_001272971.1:p.Leu255Ser
|
|
|
NM_001286043.1:c.971T>C
|
NP_001272972.1:p.Leu324Ser
|
|
|
NM_001286044.1:c.305T>C
|
NP_001272973.1:p.Leu102Ser
|
|
|
NM_000016.6:c.872T>C
MANE Select
|
NP_000007.1:p.Leu291Ser
|
|
|
NM_001127328.3:c.884T>C
|
NP_001120800.1:p.Leu295Ser
|
|
|
NM_001286042.2:c.764T>C
|
NP_001272971.1:p.Leu255Ser
|
|
|
NM_001286043.2:c.971T>C
|
NP_001272972.1:p.Leu324Ser
|
|
|
NM_001286044.2:c.305T>C
|
NP_001272973.1:p.Leu102Ser
|
|
