ENST00000311946.8:c.168C=
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Phe56=
|
|
ENST00000435489.7:c.168C=
(NIPAL4)
|
ENSP00000406456.3:p.Phe56=
|
|
ENST00000311946.7:c.354C=
(NIPAL4)
|
ENSP00000311687.7:p.Phe118=
|
|
ENST00000435489.6:c.354C=
(NIPAL4)
|
ENSP00000406456.2:p.Phe118=
|
|
ENST00000517951.5:c.*1741+25041G=
(ADAM19)
|
ENSP00000428376.1:n.*1741+25041G=
|
|
ENST00000519150.1:c.266C=
(NIPAL4)
|
ENSP00000430810.1:p.Ser89=
|
|
ENST00000519946.1:n.382C=
(NIPAL4)
|
|
|
ENST00000521390.5:n.273C=
(NIPAL4)
|
|
|
NM_001099287.1:c.354C=
(NIPAL4)
|
NP_001092757.1:p.Phe118=
|
|
NM_001172292.1:c.354C=
(NIPAL4)
|
NP_001165763.1:p.Phe118=
|
|
XM_011534552.1:c.-142C=
(NIPAL4)
|
XP_011532854.1:n.-142C=
|
|
XM_024446043.1:c.-289C=
(NIPAL4)
|
XP_024301811.1:n.-289C=
|
|
NM_001099287.2:c.168C=
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Phe56=
|
|