ENST00000264380.9:c.3393T>A
MANE Select
|
ENSP00000264380.4:p.His1131Gln
|
|
ENST00000264380.8:c.3393T>A
|
ENSP00000264380.4:p.His1131Gln
|
|
ENST00000452564.1:c.3225T>A
|
ENSP00000405736.1:p.His1075Gln
|
|
NM_015040.3:c.3393T>A
|
NP_055855.2:p.His1131Gln
|
|
XM_011510778.1:c.3429T>A
|
XP_011509080.1:p.His1143Gln
|
|
XM_011510779.1:c.3429T>A
|
XP_011509081.1:p.His1143Gln
|
|
XM_011510780.1:c.3426T>A
|
XP_011509082.1:p.His1142Gln
|
|
XM_011510781.1:c.3411T>A
|
XP_011509083.1:p.His1137Gln
|
|
XM_011510782.1:c.3429T>A
|
XP_011509084.1:p.His1143Gln
|
|
XM_011510783.1:c.3261T>A
|
XP_011509085.1:p.His1087Gln
|
|
XM_011510784.1:c.3258T>A
|
XP_011509086.1:p.His1086Gln
|
|
XM_011510785.1:c.3243T>A
|
XP_011509087.1:p.His1081Gln
|
|
XM_011510786.1:c.3138T>A
|
XP_011509088.1:p.His1046Gln
|
|
XM_011510787.1:c.3135T>A
|
XP_011509089.1:p.His1045Gln
|
|
XM_011510788.1:c.3102T>A
|
XP_011509090.1:p.His1034Gln
|
|
XM_011510789.1:c.2952T>A
|
XP_011509091.1:p.His984Gln
|
|
XM_011510790.1:c.2436T>A
|
XP_011509092.1:p.His812Gln
|
|
XM_011510791.1:c.2436T>A
|
XP_011509093.1:p.His812Gln
|
|
XM_011510792.1:c.3429T>A
|
XP_011509094.1:p.His1143Gln
|
|
XR_922888.1:n.3566T>A
|
|
|
XM_011510778.3:c.3429T>A
|
XP_011509080.1:p.His1143Gln
|
|
XM_011510779.2:c.3429T>A
|
XP_011509081.1:p.His1143Gln
|
|
XM_011510780.2:c.3426T>A
|
XP_011509082.1:p.His1142Gln
|
|
XM_011510781.3:c.3411T>A
|
XP_011509083.1:p.His1137Gln
|
|
XM_011510782.3:c.3429T>A
|
XP_011509084.1:p.His1143Gln
|
|
XM_011510783.3:c.3261T>A
|
XP_011509085.1:p.His1087Gln
|
|
XM_011510784.2:c.3258T>A
|
XP_011509086.1:p.His1086Gln
|
|
XM_011510785.3:c.3243T>A
|
XP_011509087.1:p.His1081Gln
|
|
XM_011510786.3:c.3138T>A
|
XP_011509088.1:p.His1046Gln
|
|
XM_011510789.2:c.2952T>A
|
XP_011509091.1:p.His984Gln
|
|
XM_011510792.3:c.3429T>A
|
XP_011509094.1:p.His1143Gln
|
|
XM_017003568.1:c.3375T>A
|
XP_016859057.1:p.His1125Gln
|
|
XM_017003569.1:c.3207T>A
|
XP_016859058.1:p.His1069Gln
|
|
XM_017003570.1:c.2934T>A
|
XP_016859059.1:p.His978Gln
|
|
XM_017003571.1:c.2784T>A
|
XP_016859060.1:p.His928Gln
|
|
XM_017003572.1:c.2436T>A
|
XP_016859061.1:p.His812Gln
|
|
XM_017003573.1:c.2436T>A
|
XP_016859062.1:p.His812Gln
|
|
XM_017003574.1:c.2436T>A
|
XP_016859063.1:p.His812Gln
|
|
NM_015040.4:c.3393T>A
MANE Select
|
NP_055855.2:p.His1131Gln
|
|