ENST00000264380.9:c.3395A>G
MANE Select
|
ENSP00000264380.4:p.Glu1132Gly
|
|
ENST00000264380.8:c.3395A>G
|
ENSP00000264380.4:p.Glu1132Gly
|
|
ENST00000452564.1:c.3227A>G
|
ENSP00000405736.1:p.Glu1076Gly
|
|
NM_015040.3:c.3395A>G
|
NP_055855.2:p.Glu1132Gly
|
|
XM_011510778.1:c.3431A>G
|
XP_011509080.1:p.Glu1144Gly
|
|
XM_011510779.1:c.3431A>G
|
XP_011509081.1:p.Glu1144Gly
|
|
XM_011510780.1:c.3428A>G
|
XP_011509082.1:p.Glu1143Gly
|
|
XM_011510781.1:c.3413A>G
|
XP_011509083.1:p.Glu1138Gly
|
|
XM_011510782.1:c.3431A>G
|
XP_011509084.1:p.Glu1144Gly
|
|
XM_011510783.1:c.3263A>G
|
XP_011509085.1:p.Glu1088Gly
|
|
XM_011510784.1:c.3260A>G
|
XP_011509086.1:p.Glu1087Gly
|
|
XM_011510785.1:c.3245A>G
|
XP_011509087.1:p.Glu1082Gly
|
|
XM_011510786.1:c.3140A>G
|
XP_011509088.1:p.Glu1047Gly
|
|
XM_011510787.1:c.3137A>G
|
XP_011509089.1:p.Glu1046Gly
|
|
XM_011510788.1:c.3104A>G
|
XP_011509090.1:p.Glu1035Gly
|
|
XM_011510789.1:c.2954A>G
|
XP_011509091.1:p.Glu985Gly
|
|
XM_011510790.1:c.2438A>G
|
XP_011509092.1:p.Glu813Gly
|
|
XM_011510791.1:c.2438A>G
|
XP_011509093.1:p.Glu813Gly
|
|
XM_011510792.1:c.3431A>G
|
XP_011509094.1:p.Glu1144Gly
|
|
XR_922888.1:n.3568A>G
|
|
|
XM_011510778.3:c.3431A>G
|
XP_011509080.1:p.Glu1144Gly
|
|
XM_011510779.2:c.3431A>G
|
XP_011509081.1:p.Glu1144Gly
|
|
XM_011510780.2:c.3428A>G
|
XP_011509082.1:p.Glu1143Gly
|
|
XM_011510781.3:c.3413A>G
|
XP_011509083.1:p.Glu1138Gly
|
|
XM_011510782.3:c.3431A>G
|
XP_011509084.1:p.Glu1144Gly
|
|
XM_011510783.3:c.3263A>G
|
XP_011509085.1:p.Glu1088Gly
|
|
XM_011510784.2:c.3260A>G
|
XP_011509086.1:p.Glu1087Gly
|
|
XM_011510785.3:c.3245A>G
|
XP_011509087.1:p.Glu1082Gly
|
|
XM_011510786.3:c.3140A>G
|
XP_011509088.1:p.Glu1047Gly
|
|
XM_011510789.2:c.2954A>G
|
XP_011509091.1:p.Glu985Gly
|
|
XM_011510792.3:c.3431A>G
|
XP_011509094.1:p.Glu1144Gly
|
|
XM_017003568.1:c.3377A>G
|
XP_016859057.1:p.Glu1126Gly
|
|
XM_017003569.1:c.3209A>G
|
XP_016859058.1:p.Glu1070Gly
|
|
XM_017003570.1:c.2936A>G
|
XP_016859059.1:p.Glu979Gly
|
|
XM_017003571.1:c.2786A>G
|
XP_016859060.1:p.Glu929Gly
|
|
XM_017003572.1:c.2438A>G
|
XP_016859061.1:p.Glu813Gly
|
|
XM_017003573.1:c.2438A>G
|
XP_016859062.1:p.Glu813Gly
|
|
XM_017003574.1:c.2438A>G
|
XP_016859063.1:p.Glu813Gly
|
|
NM_015040.4:c.3395A>G
MANE Select
|
NP_055855.2:p.Glu1132Gly
|
|