ENST00000311946.8:c.141G>A
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Gln47=
|
|
ENST00000435489.7:c.141G>A
(NIPAL4)
|
ENSP00000406456.3:p.Gln47=
|
|
ENST00000311946.7:c.327G>A
(NIPAL4)
|
ENSP00000311687.7:p.Gln109=
|
|
ENST00000435489.6:c.327G>A
(NIPAL4)
|
ENSP00000406456.2:p.Gln109=
|
|
ENST00000517951.5:c.*1741+25068C>T
(ADAM19)
|
ENSP00000428376.1:n.*1741+25068C>T
|
|
ENST00000519150.1:c.239G>A
(NIPAL4)
|
ENSP00000430810.1:p.Arg80Lys
|
|
ENST00000519946.1:n.355G>A
(NIPAL4)
|
|
|
ENST00000521390.5:n.246G>A
(NIPAL4)
|
|
|
NM_001099287.1:c.327G>A
(NIPAL4)
|
NP_001092757.1:p.Gln109=
|
|
NM_001172292.1:c.327G>A
(NIPAL4)
|
NP_001165763.1:p.Gln109=
|
|
XM_011534552.1:c.-169G>A
(NIPAL4)
|
XP_011532854.1:n.-169G>A
|
|
XM_024446043.1:c.-316G>A
(NIPAL4)
|
XP_024301811.1:n.-316G>A
|
|
NM_001099287.2:c.141G>A
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Gln47=
|
|