ENST00000316891.10:c.928+3G>C
MANE Select
|
ENSP00000321810.5:n.928+3G>C
|
|
ENST00000648678.1:c.1820+3G>C
|
ENSP00000497805.1:n.1820+3G>C
|
|
ENST00000316891.9:c.928+3G>C
|
ENSP00000321810.5:n.928+3G>C
|
|
ENST00000372818.5:c.928+3G>C
|
ENSP00000361905.1:n.928+3G>C
|
|
ENST00000441669.6:c.682+3G>C
|
ENSP00000388333.2:n.682+3G>C
|
|
ENST00000462797.5:c.928+3G>C
|
ENSP00000473773.1:n.928+3G>C
|
|
ENST00000465417.5:n.113-248G>C
|
|
|
ENST00000467774.1:n.210+3G>C
|
|
|
ENST00000486825.6:c.833+3G>C
|
|
|
ENST00000489945.5:c.*346+3G>C
|
ENSP00000473745.1:n.*346+3G>C
|
|
ENST00000491865.5:n.164-248G>C
|
|
|
ENST00000492612.6:c.772+3G>C
|
|
|
ENST00000495175.6:c.*350+3G>C
|
ENSP00000474264.1:n.*350+3G>C
|
|
ENST00000537440.5:c.17-248G>C
|
ENSP00000437700.1:n.17-248G>C
|
|
ENST00000541099.5:c.-140-2905G>C
|
ENSP00000437896.1:n.-140-2905G>C
|
|
NM_001312691.1:c.928+3G>C
|
NP_001299620.1:n.928+3G>C
|
|
NM_001312692.1:c.682+3G>C
|
NP_001299621.1:n.682+3G>C
|
|
NM_017646.4:c.928+3G>C
|
NP_060116.2:n.928+3G>C
|
|
NM_017646.5:c.928+3G>C
|
NP_060116.2:n.928+3G>C
|
|
NR_132401.1:n.944+3G>C
|
|
|
NR_132402.1:n.802+3G>C
|
|
|
NR_132403.1:n.798+3G>C
|
|
|
NR_132404.1:n.798+3G>C
|
|
|
NR_132405.1:n.794+3G>C
|
|
|
NR_132406.1:n.686-248G>C
|
|
|
NR_132407.1:n.562+3G>C
|
|
|
NR_132408.1:n.558+3G>C
|
|
|
NR_132409.1:n.419+3G>C
|
|
|
NR_132410.1:n.446-248G>C
|
|
|
NR_132412.1:n.307-248G>C
|
|
|
NR_132413.1:n.195-2905G>C
|
|
|
NR_132414.1:n.195-5632G>C
|
|
|
NR_132415.1:n.1035+3G>C
|
|
|
XM_005270954.1:c.685+3G>C
|
XP_005271011.1:n.685+3G>C
|
|
XM_006710706.1:c.505+3G>C
|
XP_006710769.1:n.505+3G>C
|
|
XM_005270954.2:c.685+3G>C
|
XP_005271011.1:n.685+3G>C
|
|
XR_946672.2:n.1028+3G>C
|
|
|
NM_017646.6:c.928+3G>C
MANE Select
|
NP_060116.2:n.928+3G>C
|
|