ENST00000480188.2:n.1368G>A
|
|
|
ENST00000696279.1:c.4654G>A
|
|
|
ENST00000696280.1:n.4423G>A
|
|
|
ENST00000696281.1:c.4352G>A
|
ENSP00000512521.1:p.Gly1451Glu
|
|
ENST00000697921.1:n.3212G>A
|
|
|
ENST00000697922.1:c.*4324G>A
|
ENSP00000513478.1:n.*4324G>A
|
|
ENST00000697923.1:n.4779G>A
|
|
|
ENST00000223642.3:c.4334G>A
MANE Select
|
ENSP00000223642.1:p.Gly1445Glu
|
|
ENST00000223642.2:c.4334G>A
|
ENSP00000223642.1:p.Gly1445Glu
|
|
NM_001735.2:c.4334G>A , LRG_28t1:c.4334G>A
|
NP_001726.2:p.Gly1445Glu
|
|
XM_011518980.1:c.4349G>A
|
XP_011517282.1:p.Gly1450Glu
|
|
NM_001317163.1:c.4352G>A
|
NP_001304092.1:p.Gly1451Glu
|
|
NM_001317163.2:c.4352G>A
|
NP_001304092.1:p.Gly1451Glu
|
|
NM_001735.3:c.4334G>A
MANE Select
|
NP_001726.2:p.Gly1445Glu
|
|