|
ENST00000370841.9:c.440G>C
MANE Select
|
ENSP00000359878.5:p.Gly147Ala
|
|
|
ENST00000473018.3:n.2564G>C
|
|
|
|
ENST00000525881.6:n.1402G>C
|
|
|
|
ENST00000541113.6:c.440G>C
|
ENSP00000442324.2:p.Gly147Ala
|
|
|
ENST00000679509.1:n.1402G>C
|
|
|
|
ENST00000679530.1:c.*208G>C
|
ENSP00000506454.1:n.*208G>C
|
|
|
ENST00000679615.1:n.2564G>C
|
|
|
|
ENST00000679687.1:c.31-5137G>C
|
ENSP00000506598.1:n.31-5137G>C
|
|
|
ENST00000679704.1:c.*206G>C
|
ENSP00000505117.1:n.*206G>C
|
|
|
ENST00000679709.1:c.*403G>C
|
ENSP00000506623.1:n.*403G>C
|
|
|
ENST00000679804.1:n.207+1921G>C
|
|
|
|
ENST00000679976.1:c.*24G>C
|
ENSP00000505565.1:n.*24G>C
|
|
|
ENST00000680166.1:n.3729G>C
|
|
|
|
ENST00000680517.1:c.286+1921G>C
|
ENSP00000505803.1:n.286+1921G>C
|
|
|
ENST00000680582.1:n.1402G>C
|
|
|
|
ENST00000680613.1:c.440G>C
|
ENSP00000506114.1:p.Gly147Ala
|
|
|
ENST00000680662.1:c.*354G>C
|
ENSP00000505080.1:n.*354G>C
|
|
|
ENST00000680691.1:c.*103G>C
|
ENSP00000506487.1:n.*103G>C
|
|
|
ENST00000680694.1:c.*24G>C
|
ENSP00000505658.1:n.*24G>C
|
|
|
ENST00000680743.1:c.*107G>C
|
ENSP00000505073.1:n.*107G>C
|
|
|
ENST00000680749.1:c.440G>C
|
ENSP00000505122.1:p.Gly147Ala
|
|
|
ENST00000680798.1:c.*24G>C
|
ENSP00000505670.1:n.*24G>C
|
|
|
ENST00000680805.1:c.440G>C
|
ENSP00000505447.1:p.Gly147Ala
|
|
|
ENST00000680844.1:c.*224G>C
|
ENSP00000506541.1:n.*224G>C
|
|
|
ENST00000680948.1:c.*307G>C
|
ENSP00000505441.1:n.*307G>C
|
|
|
ENST00000680964.1:c.440G>C
|
ENSP00000505961.1:p.Gly147Ala
|
|
|
ENST00000681037.1:c.440G>C
|
ENSP00000506025.1:p.Gly147Ala
|
|
|
ENST00000681063.1:c.440G>C
|
ENSP00000506616.1:p.Gly147Ala
|
|
|
ENST00000681209.1:c.*204G>C
|
ENSP00000505877.1:n.*204G>C
|
|
|
ENST00000681278.1:n.797G>C
|
|
|
|
ENST00000681289.1:n.797G>C
|
|
|
|
ENST00000681361.1:c.*107G>C
|
ENSP00000506679.1:n.*107G>C
|
|
|
ENST00000681430.1:c.440G>C
|
ENSP00000506301.1:p.Gly147Ala
|
|
|
ENST00000681446.1:c.*24G>C
|
ENSP00000506244.1:n.*24G>C
|
|
|
ENST00000681450.1:c.*107G>C
|
ENSP00000505660.1:n.*107G>C
|
|
|
ENST00000681548.1:c.*54+1921G>C
|
ENSP00000505275.1:n.*54+1921G>C
|
|
|
ENST00000681616.1:c.*208G>C
|
ENSP00000505111.1:n.*208G>C
|
|
|
ENST00000681621.1:c.*24G>C
|
ENSP00000505770.1:n.*24G>C
|
|
|
ENST00000681680.1:n.2564G>C
|
|
|
|
ENST00000681720.1:c.*54+1921G>C
|
ENSP00000505438.1:n.*54+1921G>C
|
|
|
ENST00000681730.1:n.662G>C
|
|
|
|
ENST00000681790.1:c.182G>C
|
ENSP00000505130.1:p.Gly61Ala
|
|
|
ENST00000681837.1:n.1056G>C
|
|
|
|
ENST00000681913.1:n.2564G>C
|
|
|
|
ENST00000681916.1:c.*208G>C
|
ENSP00000506477.1:n.*208G>C
|
|
|
ENST00000681930.1:n.2564G>C
|
|
|
|
ENST00000370834.9:c.539G>C
|
ENSP00000359871.5:p.Gly180Ala
|
|
|
ENST00000370841.8:c.440G>C
|
ENSP00000359878.4:p.Gly147Ala
|
|
|
ENST00000420607.6:c.452G>C
|
ENSP00000409612.2:p.Gly151Ala
|
|
|
ENST00000525808.5:c.*54+1921G>C
|
ENSP00000434823.1:n.*54+1921G>C
|
|
|
ENST00000526129.5:c.*224G>C
|
ENSP00000434092.1:n.*224G>C
|
|
|
ENST00000526196.5:c.*208G>C
|
ENSP00000431953.1:n.*208G>C
|
|
|
ENST00000526930.1:n.213G>C
|
|
|
|
ENST00000529059.5:n.349G>C
|
|
|
|
ENST00000530953.6:c.119-5137G>C
|
ENSP00000431372.1:n.119-5137G>C
|
|
|
ENST00000532509.5:c.*204G>C
|
ENSP00000432522.1:n.*204G>C
|
|
|
ENST00000534334.5:c.*24G>C
|
ENSP00000435584.1:n.*24G>C
|
|
|
ENST00000541113.5:c.332G>C
|
ENSP00000442324.1:p.Gly111Ala
|
|
|
NM_000016.5:c.440G>C
|
NP_000007.1:p.Gly147Ala
|
|
|
NM_001127328.2:c.452G>C
|
NP_001120800.1:p.Gly151Ala
|
|
|
NM_001286042.1:c.332G>C
|
NP_001272971.1:p.Gly111Ala
|
|
|
NM_001286043.1:c.539G>C
|
NP_001272972.1:p.Gly180Ala
|
|
|
NM_001286044.1:c.-100+1921G>C
|
NP_001272973.1:n.-100+1921G>C
|
|
|
NM_000016.6:c.440G>C
MANE Select
|
NP_000007.1:p.Gly147Ala
|
|
|
NM_001127328.3:c.452G>C
|
NP_001120800.1:p.Gly151Ala
|
|
|
NM_001286042.2:c.332G>C
|
NP_001272971.1:p.Gly111Ala
|
|
|
NM_001286043.2:c.539G>C
|
NP_001272972.1:p.Gly180Ala
|
|
|
NM_001286044.2:c.-100+1921G>C
|
NP_001272973.1:n.-100+1921G>C
|
|
