ENST00000378993.6:c.911+77G>A
MANE Select
|
ENSP00000368278.1:n.911+77G>A
|
|
ENST00000302196.5:c.134+77G>A
|
ENSP00000305200.5:n.134+77G>A
|
|
ENST00000378993.5:c.911+77G>A
|
ENSP00000368278.1:n.911+77G>A
|
|
NM_014271.3:c.911+77G>A
|
NP_055086.1:n.911+77G>A
|
|
XM_005274441.1:c.911+77G>A
|
XP_005274498.1:n.911+77G>A
|
|
XM_011545445.1:c.911+77G>A
|
XP_011543747.1:n.911+77G>A
|
|
XM_017029240.1:c.911+77G>A
|
XP_016884729.1:n.911+77G>A
|
|
XM_017029241.1:c.533+77G>A
|
XP_016884730.1:n.533+77G>A
|
|
NM_014271.4:c.911+77G>A
MANE Select
|
NP_055086.1:n.911+77G>A
|
|