|
ENST00000370841.9:c.1025G>C
MANE Select
|
ENSP00000359878.5:p.Trp342Ser
|
|
|
ENST00000473018.3:n.3149G>C
|
|
|
|
ENST00000532207.6:n.2036G>C
|
|
|
|
ENST00000541113.6:c.929G>C
|
ENSP00000442324.2:p.Trp310Ser
|
|
|
ENST00000679509.1:n.1987G>C
|
|
|
|
ENST00000679530.1:c.*793G>C
|
ENSP00000506454.1:n.*793G>C
|
|
|
ENST00000679615.1:n.3040G>C
|
|
|
|
ENST00000679687.1:c.587G>C
|
ENSP00000506598.1:p.Trp196Ser
|
|
|
ENST00000679704.1:c.*791G>C
|
ENSP00000505117.1:n.*791G>C
|
|
|
ENST00000679709.1:c.*988G>C
|
ENSP00000506623.1:n.*988G>C
|
|
|
ENST00000679976.1:c.*609G>C
|
ENSP00000505565.1:n.*609G>C
|
|
|
ENST00000680166.1:n.4314G>C
|
|
|
|
ENST00000680315.1:n.908G>C
|
|
|
|
ENST00000680517.1:c.*413G>C
|
ENSP00000505803.1:n.*413G>C
|
|
|
ENST00000680582.1:n.1987G>C
|
|
|
|
ENST00000680613.1:c.*518G>C
|
ENSP00000506114.1:n.*518G>C
|
|
|
ENST00000680662.1:c.*939G>C
|
ENSP00000505080.1:n.*939G>C
|
|
|
ENST00000680691.1:c.*688G>C
|
ENSP00000506487.1:n.*688G>C
|
|
|
ENST00000680694.1:c.*613G>C
|
ENSP00000505658.1:n.*613G>C
|
|
|
ENST00000680743.1:c.*814G>C
|
ENSP00000505073.1:n.*814G>C
|
|
|
ENST00000680749.1:c.*310G>C
|
ENSP00000505122.1:n.*310G>C
|
|
|
ENST00000680798.1:c.*500G>C
|
ENSP00000505670.1:n.*500G>C
|
|
|
ENST00000680805.1:c.884G>C
|
ENSP00000505447.1:p.Trp295Ser
|
|
|
ENST00000680844.1:c.*809G>C
|
ENSP00000506541.1:n.*809G>C
|
|
|
ENST00000680948.1:c.*892G>C
|
ENSP00000505441.1:n.*892G>C
|
|
|
ENST00000680964.1:c.*118G>C
|
ENSP00000505961.1:n.*118G>C
|
|
|
ENST00000681037.1:c.*2509G>C
|
ENSP00000506025.1:n.*2509G>C
|
|
|
ENST00000681063.1:c.*294G>C
|
ENSP00000506616.1:n.*294G>C
|
|
|
ENST00000681209.1:c.*680G>C
|
ENSP00000505877.1:n.*680G>C
|
|
|
ENST00000681278.1:n.1727G>C
|
|
|
|
ENST00000681289.1:n.5020G>C
|
|
|
|
ENST00000681361.1:c.*692G>C
|
ENSP00000506679.1:n.*692G>C
|
|
|
ENST00000681430.1:c.*118G>C
|
ENSP00000506301.1:n.*118G>C
|
|
|
ENST00000681446.1:c.*729G>C
|
ENSP00000506244.1:n.*729G>C
|
|
|
ENST00000681450.1:c.*696G>C
|
ENSP00000505660.1:n.*696G>C
|
|
|
ENST00000681548.1:c.*611G>C
|
ENSP00000505275.1:n.*611G>C
|
|
|
ENST00000681616.1:c.*684G>C
|
ENSP00000505111.1:n.*684G>C
|
|
|
ENST00000681621.1:c.*609G>C
|
ENSP00000505770.1:n.*609G>C
|
|
|
ENST00000681680.1:n.3120G>C
|
|
|
|
ENST00000681720.1:c.*480G>C
|
ENSP00000505438.1:n.*480G>C
|
|
|
ENST00000681730.1:n.1247G>C
|
|
|
|
ENST00000681790.1:c.767G>C
|
ENSP00000505130.1:p.Trp256Ser
|
|
|
ENST00000681837.1:n.1641G>C
|
|
|
|
ENST00000681913.1:n.3271G>C
|
|
|
|
ENST00000681916.1:c.*793G>C
|
ENSP00000506477.1:n.*793G>C
|
|
|
ENST00000681930.1:n.3149G>C
|
|
|
|
ENST00000370834.9:c.1124G>C
|
ENSP00000359871.5:p.Trp375Ser
|
|
|
ENST00000370841.8:c.1025G>C
|
ENSP00000359878.4:p.Trp342Ser
|
|
|
ENST00000420607.6:c.1037G>C
|
ENSP00000409612.2:p.Trp346Ser
|
|
|
ENST00000481374.1:n.298G>C
|
|
|
|
ENST00000525808.5:c.*611G>C
|
ENSP00000434823.1:n.*611G>C
|
|
|
ENST00000526129.5:c.*809G>C
|
ENSP00000434092.1:n.*809G>C
|
|
|
ENST00000526196.5:c.*793G>C
|
ENSP00000431953.1:n.*793G>C
|
|
|
ENST00000528016.1:c.160-7976G>C
|
ENSP00000434284.1:n.160-7976G>C
|
|
|
ENST00000529059.5:n.934G>C
|
|
|
|
ENST00000532207.5:n.755G>C
|
|
|
|
ENST00000534334.5:c.*766G>C
|
ENSP00000435584.1:n.*766G>C
|
|
|
ENST00000541113.5:c.917G>C
|
ENSP00000442324.1:p.Trp306Ser
|
|
|
NM_000016.5:c.1025G>C
|
NP_000007.1:p.Trp342Ser
|
|
|
NM_001127328.2:c.1037G>C
|
NP_001120800.1:p.Trp346Ser
|
|
|
NM_001286042.1:c.917G>C
|
NP_001272971.1:p.Trp306Ser
|
|
|
NM_001286043.1:c.1124G>C
|
NP_001272972.1:p.Trp375Ser
|
|
|
NM_001286044.1:c.458G>C
|
NP_001272973.1:p.Trp153Ser
|
|
|
NM_000016.6:c.1025G>C
MANE Select
|
NP_000007.1:p.Trp342Ser
|
|
|
NM_001127328.3:c.1037G>C
|
NP_001120800.1:p.Trp346Ser
|
|
|
NM_001286042.2:c.917G>C
|
NP_001272971.1:p.Trp306Ser
|
|
|
NM_001286043.2:c.1124G>C
|
NP_001272972.1:p.Trp375Ser
|
|
|
NM_001286044.2:c.458G>C
|
NP_001272973.1:p.Trp153Ser
|
|
