ENST00000311946.8:c.549T>A
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Thr183=
|
|
ENST00000435489.7:c.492T>A
(NIPAL4)
|
ENSP00000406456.3:p.Thr164=
|
|
ENST00000311946.7:c.735T>A
(NIPAL4)
|
ENSP00000311687.7:p.Thr245=
|
|
ENST00000435489.6:c.678T>A
(NIPAL4)
|
ENSP00000406456.2:p.Thr226=
|
|
ENST00000517951.5:c.*1741+16485A>T
(ADAM19)
|
ENSP00000428376.1:n.*1741+16485A>T
|
|
ENST00000519150.1:c.647T>A
(NIPAL4)
|
ENSP00000430810.1:n.647T>A
|
|
NM_001099287.1:c.735T>A
(NIPAL4)
|
NP_001092757.1:p.Thr245=
|
|
NM_001172292.1:c.678T>A
(NIPAL4)
|
NP_001165763.1:p.Thr226=
|
|
XM_011534552.1:c.240T>A
(NIPAL4)
|
XP_011532854.1:p.Thr80=
|
|
XM_024446043.1:c.36T>A
(NIPAL4)
|
XP_024301811.1:p.Thr12=
|
|
NM_001099287.2:c.549T>A
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Thr183=
|
|