ENST00000264380.9:c.3434G>C
MANE Select
|
ENSP00000264380.4:p.Ser1145Thr
|
|
ENST00000264380.8:c.3434G>C
|
ENSP00000264380.4:p.Ser1145Thr
|
|
ENST00000452564.1:c.3266G>C
|
ENSP00000405736.1:p.Ser1089Thr
|
|
NM_015040.3:c.3434G>C
|
NP_055855.2:p.Ser1145Thr
|
|
XM_011510778.1:c.3470G>C
|
XP_011509080.1:p.Ser1157Thr
|
|
XM_011510779.1:c.3470G>C
|
XP_011509081.1:p.Ser1157Thr
|
|
XM_011510780.1:c.3467G>C
|
XP_011509082.1:p.Ser1156Thr
|
|
XM_011510781.1:c.3452G>C
|
XP_011509083.1:p.Ser1151Thr
|
|
XM_011510782.1:c.3470G>C
|
XP_011509084.1:p.Ser1157Thr
|
|
XM_011510783.1:c.3302G>C
|
XP_011509085.1:p.Ser1101Thr
|
|
XM_011510784.1:c.3299G>C
|
XP_011509086.1:p.Ser1100Thr
|
|
XM_011510785.1:c.3284G>C
|
XP_011509087.1:p.Ser1095Thr
|
|
XM_011510786.1:c.3179G>C
|
XP_011509088.1:p.Ser1060Thr
|
|
XM_011510787.1:c.3176G>C
|
XP_011509089.1:p.Ser1059Thr
|
|
XM_011510788.1:c.3143G>C
|
XP_011509090.1:p.Ser1048Thr
|
|
XM_011510789.1:c.2993G>C
|
XP_011509091.1:p.Ser998Thr
|
|
XM_011510790.1:c.2477G>C
|
XP_011509092.1:p.Ser826Thr
|
|
XM_011510791.1:c.2477G>C
|
XP_011509093.1:p.Ser826Thr
|
|
XM_011510792.1:c.3470G>C
|
XP_011509094.1:p.Ser1157Thr
|
|
XR_922888.1:n.3607G>C
|
|
|
XM_011510778.3:c.3470G>C
|
XP_011509080.1:p.Ser1157Thr
|
|
XM_011510779.2:c.3470G>C
|
XP_011509081.1:p.Ser1157Thr
|
|
XM_011510780.2:c.3467G>C
|
XP_011509082.1:p.Ser1156Thr
|
|
XM_011510781.3:c.3452G>C
|
XP_011509083.1:p.Ser1151Thr
|
|
XM_011510782.3:c.3470G>C
|
XP_011509084.1:p.Ser1157Thr
|
|
XM_011510783.3:c.3302G>C
|
XP_011509085.1:p.Ser1101Thr
|
|
XM_011510784.2:c.3299G>C
|
XP_011509086.1:p.Ser1100Thr
|
|
XM_011510785.3:c.3284G>C
|
XP_011509087.1:p.Ser1095Thr
|
|
XM_011510786.3:c.3179G>C
|
XP_011509088.1:p.Ser1060Thr
|
|
XM_011510789.2:c.2993G>C
|
XP_011509091.1:p.Ser998Thr
|
|
XM_011510792.3:c.3470G>C
|
XP_011509094.1:p.Ser1157Thr
|
|
XM_017003568.1:c.3416G>C
|
XP_016859057.1:p.Ser1139Thr
|
|
XM_017003569.1:c.3248G>C
|
XP_016859058.1:p.Ser1083Thr
|
|
XM_017003570.1:c.2975G>C
|
XP_016859059.1:p.Ser992Thr
|
|
XM_017003571.1:c.2825G>C
|
XP_016859060.1:p.Ser942Thr
|
|
XM_017003572.1:c.2477G>C
|
XP_016859061.1:p.Ser826Thr
|
|
XM_017003573.1:c.2477G>C
|
XP_016859062.1:p.Ser826Thr
|
|
XM_017003574.1:c.2477G>C
|
XP_016859063.1:p.Ser826Thr
|
|
NM_015040.4:c.3434G>C
MANE Select
|
NP_055855.2:p.Ser1145Thr
|
|