|
ENST00000355699.7:c.1435+75G>T
MANE Select
|
ENSP00000347927.2:n.1435+75G>T
|
|
|
ENST00000355699.6:c.1435+75G>T
|
ENSP00000347927.2:n.1435+75G>T
|
|
|
ENST00000356589.6:c.1342+75G>T
|
ENSP00000348997.2:n.1342+75G>T
|
|
|
ENST00000371916.5:c.691+75G>T
|
ENSP00000360984.2:n.691+75G>T
|
|
|
ENST00000371929.7:c.1435+75G>T
|
ENSP00000360997.3:n.1435+75G>T
|
|
|
ENST00000474918.1:c.*239+75G>T
|
ENSP00000435305.1:n.*239+75G>T
|
|
|
ENST00000485925.5:n.974-2336G>T
|
|
|
|
ENST00000495234.5:c.*719+75G>T
|
ENSP00000435274.1:n.*719+75G>T
|
|
|
NM_139025.4:c.1435+75G>T , LRG_544t1:c.1435+75G>T
|
NP_620594.1:n.1435+75G>T
|
|
|
NM_139026.4:c.1342+75G>T
|
NP_620595.1:n.1342+75G>T
|
|
|
NM_139027.4:c.1435+75G>T
|
NP_620596.2:n.1435+75G>T
|
|
|
NR_024514.2:n.993-2336G>T
|
|
|
|
XM_011518174.1:c.1045+75G>T
|
XP_011516476.1:n.1045+75G>T
|
|
|
XM_011518175.1:c.1435+75G>T
|
XP_011516477.1:n.1435+75G>T
|
|
|
XM_011518176.1:c.451+75G>T
|
XP_011516478.1:n.451+75G>T
|
|
|
XM_011518177.1:c.445+75G>T
|
XP_011516479.1:n.445+75G>T
|
|
|
XM_011518178.1:c.100+75G>T
|
XP_011516480.1:n.100+75G>T
|
|
|
XM_011518179.1:c.221+75G>T
|
XP_011516481.1:n.221+75G>T
|
|
|
XM_011518180.1:c.687-7833G>T
|
XP_011516482.1:n.687-7833G>T
|
|
|
XM_011518176.3:c.451+75G>T
|
XP_011516478.1:n.451+75G>T
|
|
|
XM_011518178.2:c.100+75G>T
|
XP_011516480.1:n.100+75G>T
|
|
|
XM_017014232.1:c.1423+75G>T
|
XP_016869721.1:n.1423+75G>T
|
|
|
XM_017014233.1:c.1045+75G>T
|
XP_016869722.1:n.1045+75G>T
|
|
|
XM_017014234.2:c.445+75G>T
|
XP_016869723.1:n.445+75G>T
|
|
|
XM_017014235.1:c.1435+75G>T
|
XP_016869724.1:n.1435+75G>T
|
|
|
XR_001746171.1:n.2660+75G>T
|
|
|
|
NM_139026.5:c.1342+75G>T
|
NP_620595.1:n.1342+75G>T
|
|
|
NM_139027.5:c.1435+75G>T
|
NP_620596.2:n.1435+75G>T
|
|
|
NM_139025.5:c.1435+75G>T
|
NP_620594.1:n.1435+75G>T
|
|
|
NM_139026.6:c.1342+75G>T
|
NP_620595.1:n.1342+75G>T
|
|
|
NM_139027.6:c.1435+75G>T
MANE Select
|
NP_620596.2:n.1435+75G>T
|
|
|
NR_024514.3:n.995-2336G>T
|
|
|
