ENST00000379984.4:c.184+3118C>T
(RS1)
MANE Select
|
ENSP00000369320.3:n.184+3118C>T
|
|
ENST00000673617.1:n.356G>A
(CDKL5)
|
|
|
ENST00000379984.3:c.184+3118C>T
(RS1)
|
ENSP00000369320.3:n.184+3118C>T
|
|
ENST00000379989.6:c.3084G>A
(CDKL5)
|
ENSP00000369325.3:p.Thr1028=
|
|
ENST00000379996.7:c.3084G>A
(CDKL5)
|
ENSP00000369332.3:p.Thr1028=
|
|
NM_000330.3:c.184+3118C>T , LRG_702t1:c.184+3118C>T
(RS1)
|
NP_000321.1:n.184+3118C>T
|
|
NM_001037343.1:c.3084G>A
(CDKL5)
|
NP_001032420.1:p.Thr1028=
|
|
NM_003159.2:c.3084G>A
(CDKL5)
|
NP_003150.1:p.Thr1028=
|
|
XM_011545569.1:c.3156G>A
(CDKL5)
|
XP_011543871.1:p.Thr1052=
|
|
XM_011545570.1:c.3075G>A
(CDKL5)
|
XP_011543872.1:p.Thr1025=
|
|
XR_950484.1:n.3459G>A
(CDKL5)
|
|
|
NM_000330.4:c.184+3118C>T
(RS1)
MANE Select
|
NP_000321.1:n.184+3118C>T
|
|
NM_001037343.2:c.3084G>A
(CDKL5)
|
NP_001032420.1:p.Thr1028=
|
|
NM_003159.3:c.3084G>A
(CDKL5)
|
NP_003150.1:p.Thr1028=
|
|