ENST00000683570.1:c.421G>T
(NPHP3)
|
ENSP00000508409.1:p.Gly141Ter
|
|
ENST00000684294.1:c.99+322G>T
(NPHP3)
|
ENSP00000508078.1:n.99+322G>T
|
|
ENST00000684756.1:n.116+28G>T
(NPHP3)
|
|
|
ENST00000337331.10:c.393+28G>T
(NPHP3)
MANE Select
|
ENSP00000338766.5:n.393+28G>T
|
|
ENST00000337331.9:c.393+28G>T
(NPHP3)
|
ENSP00000338766.5:n.393+28G>T
|
|
ENST00000383282.3:c.393+28G>T
(NPHP3-ACAD11)
|
ENSP00000372769.2:n.393+28G>T
|
|
ENST00000465756.5:c.99+322G>T
(NPHP3)
|
ENSP00000419907.1:n.99+322G>T
|
|
ENST00000469232.5:c.45+28G>T
(NPHP3)
|
ENSP00000418664.1:n.45+28G>T
|
|
ENST00000471702.2:c.393+28G>T
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.393+28G>T
|
|
NM_153240.4:c.393+28G>T
(NPHP3)
|
NP_694972.3:n.393+28G>T
|
|
NR_037804.1:n.497+28G>T
(NPHP3-ACAD11)
|
|
|
NR_002811.2:n.186C>A
(NPHP3-AS1)
|
|
|
NR_152743.1:n.186C>A
(NPHP3-AS1)
|
|
|
NM_153240.5:c.393+28G>T
(NPHP3)
MANE Select
|
NP_694972.3:n.393+28G>T
|
|