|
ENST00000370841.9:c.851T>C
MANE Select
|
ENSP00000359878.5:p.Val284Ala
|
|
|
ENST00000473018.3:n.2975T>C
|
|
|
|
ENST00000532207.6:n.1740T>C
|
|
|
|
ENST00000541113.6:c.849+893T>C
|
ENSP00000442324.2:n.849+893T>C
|
|
|
ENST00000679509.1:n.1813T>C
|
|
|
|
ENST00000679530.1:c.*619T>C
|
ENSP00000506454.1:n.*619T>C
|
|
|
ENST00000679615.1:n.2866T>C
|
|
|
|
ENST00000679687.1:c.413T>C
|
ENSP00000506598.1:p.Val138Ala
|
|
|
ENST00000679704.1:c.*617T>C
|
ENSP00000505117.1:n.*617T>C
|
|
|
ENST00000679709.1:c.*814T>C
|
ENSP00000506623.1:n.*814T>C
|
|
|
ENST00000679976.1:c.*435T>C
|
ENSP00000505565.1:n.*435T>C
|
|
|
ENST00000680166.1:n.4140T>C
|
|
|
|
ENST00000680315.1:n.734T>C
|
|
|
|
ENST00000680517.1:c.*239T>C
|
ENSP00000505803.1:n.*239T>C
|
|
|
ENST00000680582.1:n.1813T>C
|
|
|
|
ENST00000680613.1:c.*222T>C
|
ENSP00000506114.1:n.*222T>C
|
|
|
ENST00000680662.1:c.*765T>C
|
ENSP00000505080.1:n.*765T>C
|
|
|
ENST00000680691.1:c.*514T>C
|
ENSP00000506487.1:n.*514T>C
|
|
|
ENST00000680694.1:c.*439T>C
|
ENSP00000505658.1:n.*439T>C
|
|
|
ENST00000680743.1:c.*518T>C
|
ENSP00000505073.1:n.*518T>C
|
|
|
ENST00000680749.1:c.*136T>C
|
ENSP00000505122.1:n.*136T>C
|
|
|
ENST00000680798.1:c.*326T>C
|
ENSP00000505670.1:n.*326T>C
|
|
|
ENST00000680805.1:c.710T>C
|
ENSP00000505447.1:p.Val237Ala
|
|
|
ENST00000680844.1:c.*635T>C
|
ENSP00000506541.1:n.*635T>C
|
|
|
ENST00000680948.1:c.*718T>C
|
ENSP00000505441.1:n.*718T>C
|
|
|
ENST00000680964.1:c.851T>C
|
ENSP00000505961.1:p.Val284Ala
|
|
|
ENST00000681037.1:c.*2335T>C
|
ENSP00000506025.1:n.*2335T>C
|
|
|
ENST00000681063.1:c.601T>C
|
ENSP00000506616.1:p.Ter201Gln
|
|
|
ENST00000681209.1:c.*506T>C
|
ENSP00000505877.1:n.*506T>C
|
|
|
ENST00000681278.1:n.1208T>C
|
|
|
|
ENST00000681289.1:n.4846T>C
|
|
|
|
ENST00000681361.1:c.*518T>C
|
ENSP00000506679.1:n.*518T>C
|
|
|
ENST00000681430.1:c.851T>C
|
ENSP00000506301.1:p.Val284Ala
|
|
|
ENST00000681446.1:c.*433T>C
|
ENSP00000506244.1:n.*433T>C
|
|
|
ENST00000681450.1:c.*522T>C
|
ENSP00000505660.1:n.*522T>C
|
|
|
ENST00000681548.1:c.*437T>C
|
ENSP00000505275.1:n.*437T>C
|
|
|
ENST00000681616.1:c.*510T>C
|
ENSP00000505111.1:n.*510T>C
|
|
|
ENST00000681621.1:c.*435T>C
|
ENSP00000505770.1:n.*435T>C
|
|
|
ENST00000681680.1:n.2946T>C
|
|
|
|
ENST00000681720.1:c.*306T>C
|
ENSP00000505438.1:n.*306T>C
|
|
|
ENST00000681730.1:n.1073T>C
|
|
|
|
ENST00000681790.1:c.593T>C
|
ENSP00000505130.1:p.Val198Ala
|
|
|
ENST00000681837.1:n.1467T>C
|
|
|
|
ENST00000681913.1:n.2975T>C
|
|
|
|
ENST00000681916.1:c.*619T>C
|
ENSP00000506477.1:n.*619T>C
|
|
|
ENST00000681930.1:n.2975T>C
|
|
|
|
ENST00000370834.9:c.950T>C
|
ENSP00000359871.5:p.Val317Ala
|
|
|
ENST00000370841.8:c.851T>C
|
ENSP00000359878.4:p.Val284Ala
|
|
|
ENST00000420607.6:c.863T>C
|
ENSP00000409612.2:p.Val288Ala
|
|
|
ENST00000481374.1:n.2T>C
|
|
|
|
ENST00000525808.5:c.*437T>C
|
ENSP00000434823.1:n.*437T>C
|
|
|
ENST00000526129.5:c.*635T>C
|
ENSP00000434092.1:n.*635T>C
|
|
|
ENST00000526196.5:c.*619T>C
|
ENSP00000431953.1:n.*619T>C
|
|
|
ENST00000528016.1:c.65T>C
|
ENSP00000434284.1:p.Val22Ala
|
|
|
ENST00000529059.5:n.760T>C
|
|
|
|
ENST00000532207.5:n.581T>C
|
|
|
|
ENST00000534334.5:c.*435T>C
|
ENSP00000435584.1:n.*435T>C
|
|
|
ENST00000541113.5:c.743T>C
|
ENSP00000442324.1:p.Val248Ala
|
|
|
NM_000016.5:c.851T>C
|
NP_000007.1:p.Val284Ala
|
|
|
NM_001127328.2:c.863T>C
|
NP_001120800.1:p.Val288Ala
|
|
|
NM_001286042.1:c.743T>C
|
NP_001272971.1:p.Val248Ala
|
|
|
NM_001286043.1:c.950T>C
|
NP_001272972.1:p.Val317Ala
|
|
|
NM_001286044.1:c.284T>C
|
NP_001272973.1:p.Val95Ala
|
|
|
NM_000016.6:c.851T>C
MANE Select
|
NP_000007.1:p.Val284Ala
|
|
|
NM_001127328.3:c.863T>C
|
NP_001120800.1:p.Val288Ala
|
|
|
NM_001286042.2:c.743T>C
|
NP_001272971.1:p.Val248Ala
|
|
|
NM_001286043.2:c.950T>C
|
NP_001272972.1:p.Val317Ala
|
|
|
NM_001286044.2:c.284T>C
|
NP_001272973.1:p.Val95Ala
|
|
