ENST00000311946.8:c.466C>T
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Leu156=
|
|
ENST00000435489.7:c.409C>T
(NIPAL4)
|
ENSP00000406456.3:p.Leu137=
|
|
ENST00000311946.7:c.652C>T
(NIPAL4)
|
ENSP00000311687.7:p.Leu218=
|
|
ENST00000435489.6:c.595C>T
(NIPAL4)
|
ENSP00000406456.2:p.Leu199=
|
|
ENST00000517951.5:c.*1741+16568G>A
(ADAM19)
|
ENSP00000428376.1:n.*1741+16568G>A
|
|
ENST00000519150.1:c.564C>T
(NIPAL4)
|
ENSP00000430810.1:n.564C>T
|
|
NM_001099287.1:c.652C>T
(NIPAL4)
|
NP_001092757.1:p.Leu218=
|
|
NM_001172292.1:c.595C>T
(NIPAL4)
|
NP_001165763.1:p.Leu199=
|
|
XM_011534552.1:c.157C>T
(NIPAL4)
|
XP_011532854.1:p.Leu53=
|
|
XM_024446043.1:c.-48C>T
(NIPAL4)
|
XP_024301811.1:n.-48C>T
|
|
NM_001099287.2:c.466C>T
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Leu156=
|
|