ENST00000264380.9:c.3438G>C
MANE Select
|
ENSP00000264380.4:p.Gln1146His
|
|
ENST00000264380.8:c.3438G>C
|
ENSP00000264380.4:p.Gln1146His
|
|
ENST00000452564.1:c.3270G>C
|
ENSP00000405736.1:p.Gln1090His
|
|
NM_015040.3:c.3438G>C
|
NP_055855.2:p.Gln1146His
|
|
XM_011510778.1:c.3474G>C
|
XP_011509080.1:p.Gln1158His
|
|
XM_011510779.1:c.3474G>C
|
XP_011509081.1:p.Gln1158His
|
|
XM_011510780.1:c.3471G>C
|
XP_011509082.1:p.Gln1157His
|
|
XM_011510781.1:c.3456G>C
|
XP_011509083.1:p.Gln1152His
|
|
XM_011510782.1:c.3474G>C
|
XP_011509084.1:p.Gln1158His
|
|
XM_011510783.1:c.3306G>C
|
XP_011509085.1:p.Gln1102His
|
|
XM_011510784.1:c.3303G>C
|
XP_011509086.1:p.Gln1101His
|
|
XM_011510785.1:c.3288G>C
|
XP_011509087.1:p.Gln1096His
|
|
XM_011510786.1:c.3183G>C
|
XP_011509088.1:p.Gln1061His
|
|
XM_011510787.1:c.3180G>C
|
XP_011509089.1:p.Gln1060His
|
|
XM_011510788.1:c.3147G>C
|
XP_011509090.1:p.Gln1049His
|
|
XM_011510789.1:c.2997G>C
|
XP_011509091.1:p.Gln999His
|
|
XM_011510790.1:c.2481G>C
|
XP_011509092.1:p.Gln827His
|
|
XM_011510791.1:c.2481G>C
|
XP_011509093.1:p.Gln827His
|
|
XM_011510792.1:c.3474G>C
|
XP_011509094.1:p.Gln1158His
|
|
XR_922888.1:n.3611G>C
|
|
|
XM_011510778.3:c.3474G>C
|
XP_011509080.1:p.Gln1158His
|
|
XM_011510779.2:c.3474G>C
|
XP_011509081.1:p.Gln1158His
|
|
XM_011510780.2:c.3471G>C
|
XP_011509082.1:p.Gln1157His
|
|
XM_011510781.3:c.3456G>C
|
XP_011509083.1:p.Gln1152His
|
|
XM_011510782.3:c.3474G>C
|
XP_011509084.1:p.Gln1158His
|
|
XM_011510783.3:c.3306G>C
|
XP_011509085.1:p.Gln1102His
|
|
XM_011510784.2:c.3303G>C
|
XP_011509086.1:p.Gln1101His
|
|
XM_011510785.3:c.3288G>C
|
XP_011509087.1:p.Gln1096His
|
|
XM_011510786.3:c.3183G>C
|
XP_011509088.1:p.Gln1061His
|
|
XM_011510789.2:c.2997G>C
|
XP_011509091.1:p.Gln999His
|
|
XM_011510792.3:c.3474G>C
|
XP_011509094.1:p.Gln1158His
|
|
XM_017003568.1:c.3420G>C
|
XP_016859057.1:p.Gln1140His
|
|
XM_017003569.1:c.3252G>C
|
XP_016859058.1:p.Gln1084His
|
|
XM_017003570.1:c.2979G>C
|
XP_016859059.1:p.Gln993His
|
|
XM_017003571.1:c.2829G>C
|
XP_016859060.1:p.Gln943His
|
|
XM_017003572.1:c.2481G>C
|
XP_016859061.1:p.Gln827His
|
|
XM_017003573.1:c.2481G>C
|
XP_016859062.1:p.Gln827His
|
|
XM_017003574.1:c.2481G>C
|
XP_016859063.1:p.Gln827His
|
|
NM_015040.4:c.3438G>C
MANE Select
|
NP_055855.2:p.Gln1146His
|
|