ENST00000699947.1:c.1669+5G>A
|
ENSP00000514703.1:n.1669+5G>A
|
|
ENST00000699948.1:c.1624-178G>A
|
ENSP00000514704.1:n.1624-178G>A
|
|
ENST00000382745.9:c.1669+5G>A
MANE Select
|
ENSP00000372193.4:n.1669+5G>A
|
|
ENST00000262318.12:c.1597+5G>A
|
ENSP00000262318.8:n.1597+5G>A
|
|
ENST00000382745.8:c.1669+5G>A
|
ENSP00000372193.4:n.1669+5G>A
|
|
ENST00000448525.5:c.1597+5G>A
|
ENSP00000410907.1:n.1597+5G>A
|
|
ENST00000563642.6:n.1738+5G>A
|
|
|
ENST00000565092.6:n.527G>A
|
|
|
NM_001114331.2:c.1597+5G>A
|
NP_001107803.1:n.1597+5G>A
|
|
NM_001287.5:c.1669+5G>A
|
NP_001278.1:n.1669+5G>A
|
|
XM_011522354.1:c.1495+5G>A
|
XP_011520656.1:n.1495+5G>A
|
|
NM_001287.6:c.1669+5G>A
MANE Select
|
NP_001278.1:n.1669+5G>A
|
|
NM_001114331.3:c.1597+5G>A
|
NP_001107803.1:n.1597+5G>A
|
|