ENST00000311946.8:c.564G>T
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Met188Ile
|
|
ENST00000435489.7:c.507G>T
(NIPAL4)
|
ENSP00000406456.3:p.Met169Ile
|
|
ENST00000311946.7:c.750G>T
(NIPAL4)
|
ENSP00000311687.7:p.Met250Ile
|
|
ENST00000435489.6:c.693G>T
(NIPAL4)
|
ENSP00000406456.2:p.Met231Ile
|
|
ENST00000517951.5:c.*1741+16470C>A
(ADAM19)
|
ENSP00000428376.1:n.*1741+16470C>A
|
|
ENST00000519150.1:c.662G>T
(NIPAL4)
|
ENSP00000430810.1:n.662G>T
|
|
NM_001099287.1:c.750G>T
(NIPAL4)
|
NP_001092757.1:p.Met250Ile
|
|
NM_001172292.1:c.693G>T
(NIPAL4)
|
NP_001165763.1:p.Met231Ile
|
|
XM_011534552.1:c.255G>T
(NIPAL4)
|
XP_011532854.1:p.Met85Ile
|
|
XM_024446043.1:c.51G>T
(NIPAL4)
|
XP_024301811.1:p.Met17Ile
|
|
NM_001099287.2:c.564G>T
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Met188Ile
|
|