ENST00000311946.8:c.212G>A
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Gly71Asp
|
|
ENST00000435489.7:c.212G>A
(NIPAL4)
|
ENSP00000406456.3:p.Gly71Asp
|
|
ENST00000311946.7:c.398G>A
(NIPAL4)
|
ENSP00000311687.7:p.Gly133Asp
|
|
ENST00000435489.6:c.398G>A
(NIPAL4)
|
ENSP00000406456.2:p.Gly133Asp
|
|
ENST00000517951.5:c.*1741+24997C>T
(ADAM19)
|
ENSP00000428376.1:n.*1741+24997C>T
|
|
ENST00000519150.1:c.310G>A
(NIPAL4)
|
ENSP00000430810.1:p.Ala104Thr
|
|
ENST00000519946.1:n.426G>A
(NIPAL4)
|
|
|
ENST00000521390.5:n.317G>A
(NIPAL4)
|
|
|
NM_001099287.1:c.398G>A
(NIPAL4)
|
NP_001092757.1:p.Gly133Asp
|
|
NM_001172292.1:c.398G>A
(NIPAL4)
|
NP_001165763.1:p.Gly133Asp
|
|
XM_011534552.1:c.-98G>A
(NIPAL4)
|
XP_011532854.1:n.-98G>A
|
|
XM_024446043.1:c.-245G>A
(NIPAL4)
|
XP_024301811.1:n.-245G>A
|
|
NM_001099287.2:c.212G>A
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Gly71Asp
|
|