ENST00000311946.8:c.180G>T
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Leu60=
|
|
ENST00000435489.7:c.180G>T
(NIPAL4)
|
ENSP00000406456.3:p.Leu60=
|
|
ENST00000311946.7:c.366G>T
(NIPAL4)
|
ENSP00000311687.7:p.Leu122=
|
|
ENST00000435489.6:c.366G>T
(NIPAL4)
|
ENSP00000406456.2:p.Leu122=
|
|
ENST00000517951.5:c.*1741+25029C>A
(ADAM19)
|
ENSP00000428376.1:n.*1741+25029C>A
|
|
ENST00000519150.1:c.278G>T
(NIPAL4)
|
ENSP00000430810.1:p.Trp93Leu
|
|
ENST00000519946.1:n.394G>T
(NIPAL4)
|
|
|
ENST00000521390.5:n.285G>T
(NIPAL4)
|
|
|
NM_001099287.1:c.366G>T
(NIPAL4)
|
NP_001092757.1:p.Leu122=
|
|
NM_001172292.1:c.366G>T
(NIPAL4)
|
NP_001165763.1:p.Leu122=
|
|
XM_011534552.1:c.-130G>T
(NIPAL4)
|
XP_011532854.1:n.-130G>T
|
|
XM_024446043.1:c.-277G>T
(NIPAL4)
|
XP_024301811.1:n.-277G>T
|
|
NM_001099287.2:c.180G>T
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Leu60=
|
|