ENST00000264380.9:c.3573T>C
MANE Select
|
ENSP00000264380.4:p.Asp1191=
|
|
ENST00000264380.8:c.3573T>C
|
ENSP00000264380.4:p.Asp1191=
|
|
ENST00000452564.1:c.3405T>C
|
ENSP00000405736.1:p.Asp1135=
|
|
NM_015040.3:c.3573T>C
|
NP_055855.2:p.Asp1191=
|
|
XM_011510778.1:c.3609T>C
|
XP_011509080.1:p.Asp1203=
|
|
XM_011510779.1:c.3609T>C
|
XP_011509081.1:p.Asp1203=
|
|
XM_011510780.1:c.3606T>C
|
XP_011509082.1:p.Asp1202=
|
|
XM_011510781.1:c.3591T>C
|
XP_011509083.1:p.Asp1197=
|
|
XM_011510782.1:c.3609T>C
|
XP_011509084.1:p.Asp1203=
|
|
XM_011510783.1:c.3441T>C
|
XP_011509085.1:p.Asp1147=
|
|
XM_011510784.1:c.3438T>C
|
XP_011509086.1:p.Asp1146=
|
|
XM_011510785.1:c.3423T>C
|
XP_011509087.1:p.Asp1141=
|
|
XM_011510786.1:c.3318T>C
|
XP_011509088.1:p.Asp1106=
|
|
XM_011510787.1:c.3315T>C
|
XP_011509089.1:p.Asp1105=
|
|
XM_011510788.1:c.3282T>C
|
XP_011509090.1:p.Asp1094=
|
|
XM_011510789.1:c.3132T>C
|
XP_011509091.1:p.Asp1044=
|
|
XM_011510790.1:c.2616T>C
|
XP_011509092.1:p.Asp872=
|
|
XM_011510791.1:c.2616T>C
|
XP_011509093.1:p.Asp872=
|
|
XM_011510792.1:c.3609T>C
|
XP_011509094.1:p.Asp1203=
|
|
XR_922888.1:n.3746T>C
|
|
|
XM_011510778.3:c.3609T>C
|
XP_011509080.1:p.Asp1203=
|
|
XM_011510779.2:c.3609T>C
|
XP_011509081.1:p.Asp1203=
|
|
XM_011510780.2:c.3606T>C
|
XP_011509082.1:p.Asp1202=
|
|
XM_011510781.3:c.3591T>C
|
XP_011509083.1:p.Asp1197=
|
|
XM_011510782.3:c.3609T>C
|
XP_011509084.1:p.Asp1203=
|
|
XM_011510783.3:c.3441T>C
|
XP_011509085.1:p.Asp1147=
|
|
XM_011510784.2:c.3438T>C
|
XP_011509086.1:p.Asp1146=
|
|
XM_011510785.3:c.3423T>C
|
XP_011509087.1:p.Asp1141=
|
|
XM_011510786.3:c.3318T>C
|
XP_011509088.1:p.Asp1106=
|
|
XM_011510789.2:c.3132T>C
|
XP_011509091.1:p.Asp1044=
|
|
XM_011510792.3:c.3609T>C
|
XP_011509094.1:p.Asp1203=
|
|
XM_017003568.1:c.3555T>C
|
XP_016859057.1:p.Asp1185=
|
|
XM_017003569.1:c.3387T>C
|
XP_016859058.1:p.Asp1129=
|
|
XM_017003570.1:c.3114T>C
|
XP_016859059.1:p.Asp1038=
|
|
XM_017003571.1:c.2964T>C
|
XP_016859060.1:p.Asp988=
|
|
XM_017003572.1:c.2616T>C
|
XP_016859061.1:p.Asp872=
|
|
XM_017003573.1:c.2616T>C
|
XP_016859062.1:p.Asp872=
|
|
XM_017003574.1:c.2616T>C
|
XP_016859063.1:p.Asp872=
|
|
NM_015040.4:c.3573T>C
MANE Select
|
NP_055855.2:p.Asp1191=
|
|