ENST00000264380.9:c.3421C>A
MANE Select
|
ENSP00000264380.4:p.His1141Asn
|
|
ENST00000264380.8:c.3421C>A
|
ENSP00000264380.4:p.His1141Asn
|
|
ENST00000452564.1:c.3253C>A
|
ENSP00000405736.1:p.His1085Asn
|
|
NM_015040.3:c.3421C>A
|
NP_055855.2:p.His1141Asn
|
|
XM_011510778.1:c.3457C>A
|
XP_011509080.1:p.His1153Asn
|
|
XM_011510779.1:c.3457C>A
|
XP_011509081.1:p.His1153Asn
|
|
XM_011510780.1:c.3454C>A
|
XP_011509082.1:p.His1152Asn
|
|
XM_011510781.1:c.3439C>A
|
XP_011509083.1:p.His1147Asn
|
|
XM_011510782.1:c.3457C>A
|
XP_011509084.1:p.His1153Asn
|
|
XM_011510783.1:c.3289C>A
|
XP_011509085.1:p.His1097Asn
|
|
XM_011510784.1:c.3286C>A
|
XP_011509086.1:p.His1096Asn
|
|
XM_011510785.1:c.3271C>A
|
XP_011509087.1:p.His1091Asn
|
|
XM_011510786.1:c.3166C>A
|
XP_011509088.1:p.His1056Asn
|
|
XM_011510787.1:c.3163C>A
|
XP_011509089.1:p.His1055Asn
|
|
XM_011510788.1:c.3130C>A
|
XP_011509090.1:p.His1044Asn
|
|
XM_011510789.1:c.2980C>A
|
XP_011509091.1:p.His994Asn
|
|
XM_011510790.1:c.2464C>A
|
XP_011509092.1:p.His822Asn
|
|
XM_011510791.1:c.2464C>A
|
XP_011509093.1:p.His822Asn
|
|
XM_011510792.1:c.3457C>A
|
XP_011509094.1:p.His1153Asn
|
|
XR_922888.1:n.3594C>A
|
|
|
XM_011510778.3:c.3457C>A
|
XP_011509080.1:p.His1153Asn
|
|
XM_011510779.2:c.3457C>A
|
XP_011509081.1:p.His1153Asn
|
|
XM_011510780.2:c.3454C>A
|
XP_011509082.1:p.His1152Asn
|
|
XM_011510781.3:c.3439C>A
|
XP_011509083.1:p.His1147Asn
|
|
XM_011510782.3:c.3457C>A
|
XP_011509084.1:p.His1153Asn
|
|
XM_011510783.3:c.3289C>A
|
XP_011509085.1:p.His1097Asn
|
|
XM_011510784.2:c.3286C>A
|
XP_011509086.1:p.His1096Asn
|
|
XM_011510785.3:c.3271C>A
|
XP_011509087.1:p.His1091Asn
|
|
XM_011510786.3:c.3166C>A
|
XP_011509088.1:p.His1056Asn
|
|
XM_011510789.2:c.2980C>A
|
XP_011509091.1:p.His994Asn
|
|
XM_011510792.3:c.3457C>A
|
XP_011509094.1:p.His1153Asn
|
|
XM_017003568.1:c.3403C>A
|
XP_016859057.1:p.His1135Asn
|
|
XM_017003569.1:c.3235C>A
|
XP_016859058.1:p.His1079Asn
|
|
XM_017003570.1:c.2962C>A
|
XP_016859059.1:p.His988Asn
|
|
XM_017003571.1:c.2812C>A
|
XP_016859060.1:p.His938Asn
|
|
XM_017003572.1:c.2464C>A
|
XP_016859061.1:p.His822Asn
|
|
XM_017003573.1:c.2464C>A
|
XP_016859062.1:p.His822Asn
|
|
XM_017003574.1:c.2464C>A
|
XP_016859063.1:p.His822Asn
|
|
NM_015040.4:c.3421C>A
MANE Select
|
NP_055855.2:p.His1141Asn
|
|