ENST00000311946.8:c.80G>T
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Cys27Phe
|
|
ENST00000435489.7:c.80G>T
(NIPAL4)
|
ENSP00000406456.3:p.Cys27Phe
|
|
ENST00000311946.7:c.266G>T
(NIPAL4)
|
ENSP00000311687.7:p.Cys89Phe
|
|
ENST00000435489.6:c.266G>T
(NIPAL4)
|
ENSP00000406456.2:p.Cys89Phe
|
|
ENST00000517951.5:c.*1741+25129C>A
(ADAM19)
|
ENSP00000428376.1:n.*1741+25129C>A
|
|
ENST00000519150.1:c.178G>T
(NIPAL4)
|
ENSP00000430810.1:p.Ala60Ser
|
|
ENST00000519946.1:n.294G>T
(NIPAL4)
|
|
|
ENST00000521390.5:n.185G>T
(NIPAL4)
|
|
|
NM_001099287.1:c.266G>T
(NIPAL4)
|
NP_001092757.1:p.Cys89Phe
|
|
NM_001172292.1:c.266G>T
(NIPAL4)
|
NP_001165763.1:p.Cys89Phe
|
|
XM_011534552.1:c.-230G>T
(NIPAL4)
|
XP_011532854.1:n.-230G>T
|
|
XM_024446043.1:c.-377G>T
(NIPAL4)
|
XP_024301811.1:n.-377G>T
|
|
NM_001099287.2:c.80G>T
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Cys27Phe
|
|