ENST00000264380.9:c.3394G>C
MANE Select
|
ENSP00000264380.4:p.Glu1132Gln
|
|
ENST00000264380.8:c.3394G>C
|
ENSP00000264380.4:p.Glu1132Gln
|
|
ENST00000452564.1:c.3226G>C
|
ENSP00000405736.1:p.Glu1076Gln
|
|
NM_015040.3:c.3394G>C
|
NP_055855.2:p.Glu1132Gln
|
|
XM_011510778.1:c.3430G>C
|
XP_011509080.1:p.Glu1144Gln
|
|
XM_011510779.1:c.3430G>C
|
XP_011509081.1:p.Glu1144Gln
|
|
XM_011510780.1:c.3427G>C
|
XP_011509082.1:p.Glu1143Gln
|
|
XM_011510781.1:c.3412G>C
|
XP_011509083.1:p.Glu1138Gln
|
|
XM_011510782.1:c.3430G>C
|
XP_011509084.1:p.Glu1144Gln
|
|
XM_011510783.1:c.3262G>C
|
XP_011509085.1:p.Glu1088Gln
|
|
XM_011510784.1:c.3259G>C
|
XP_011509086.1:p.Glu1087Gln
|
|
XM_011510785.1:c.3244G>C
|
XP_011509087.1:p.Glu1082Gln
|
|
XM_011510786.1:c.3139G>C
|
XP_011509088.1:p.Glu1047Gln
|
|
XM_011510787.1:c.3136G>C
|
XP_011509089.1:p.Glu1046Gln
|
|
XM_011510788.1:c.3103G>C
|
XP_011509090.1:p.Glu1035Gln
|
|
XM_011510789.1:c.2953G>C
|
XP_011509091.1:p.Glu985Gln
|
|
XM_011510790.1:c.2437G>C
|
XP_011509092.1:p.Glu813Gln
|
|
XM_011510791.1:c.2437G>C
|
XP_011509093.1:p.Glu813Gln
|
|
XM_011510792.1:c.3430G>C
|
XP_011509094.1:p.Glu1144Gln
|
|
XR_922888.1:n.3567G>C
|
|
|
XM_011510778.3:c.3430G>C
|
XP_011509080.1:p.Glu1144Gln
|
|
XM_011510779.2:c.3430G>C
|
XP_011509081.1:p.Glu1144Gln
|
|
XM_011510780.2:c.3427G>C
|
XP_011509082.1:p.Glu1143Gln
|
|
XM_011510781.3:c.3412G>C
|
XP_011509083.1:p.Glu1138Gln
|
|
XM_011510782.3:c.3430G>C
|
XP_011509084.1:p.Glu1144Gln
|
|
XM_011510783.3:c.3262G>C
|
XP_011509085.1:p.Glu1088Gln
|
|
XM_011510784.2:c.3259G>C
|
XP_011509086.1:p.Glu1087Gln
|
|
XM_011510785.3:c.3244G>C
|
XP_011509087.1:p.Glu1082Gln
|
|
XM_011510786.3:c.3139G>C
|
XP_011509088.1:p.Glu1047Gln
|
|
XM_011510789.2:c.2953G>C
|
XP_011509091.1:p.Glu985Gln
|
|
XM_011510792.3:c.3430G>C
|
XP_011509094.1:p.Glu1144Gln
|
|
XM_017003568.1:c.3376G>C
|
XP_016859057.1:p.Glu1126Gln
|
|
XM_017003569.1:c.3208G>C
|
XP_016859058.1:p.Glu1070Gln
|
|
XM_017003570.1:c.2935G>C
|
XP_016859059.1:p.Glu979Gln
|
|
XM_017003571.1:c.2785G>C
|
XP_016859060.1:p.Glu929Gln
|
|
XM_017003572.1:c.2437G>C
|
XP_016859061.1:p.Glu813Gln
|
|
XM_017003573.1:c.2437G>C
|
XP_016859062.1:p.Glu813Gln
|
|
XM_017003574.1:c.2437G>C
|
XP_016859063.1:p.Glu813Gln
|
|
NM_015040.4:c.3394G>C
MANE Select
|
NP_055855.2:p.Glu1132Gln
|
|