ENST00000311946.8:c.238G>T
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Gly80Cys
|
|
ENST00000435489.7:c.238G>T
(NIPAL4)
|
ENSP00000406456.3:p.Gly80Cys
|
|
ENST00000311946.7:c.424G>T
(NIPAL4)
|
ENSP00000311687.7:p.Gly142Cys
|
|
ENST00000435489.6:c.424G>T
(NIPAL4)
|
ENSP00000406456.2:p.Gly142Cys
|
|
ENST00000517951.5:c.*1741+24971C>A
(ADAM19)
|
ENSP00000428376.1:n.*1741+24971C>A
|
|
ENST00000519150.1:c.336G>T
(NIPAL4)
|
ENSP00000430810.1:p.Lys112Asn
|
|
ENST00000519946.1:n.452G>T
(NIPAL4)
|
|
|
ENST00000521390.5:n.343G>T
(NIPAL4)
|
|
|
NM_001099287.1:c.424G>T
(NIPAL4)
|
NP_001092757.1:p.Gly142Cys
|
|
NM_001172292.1:c.424G>T
(NIPAL4)
|
NP_001165763.1:p.Gly142Cys
|
|
XM_011534552.1:c.-72G>T
(NIPAL4)
|
XP_011532854.1:n.-72G>T
|
|
XM_024446043.1:c.-219G>T
(NIPAL4)
|
XP_024301811.1:n.-219G>T
|
|
NM_001099287.2:c.238G>T
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Gly80Cys
|
|