ENST00000684294.1:c.1366A=
(NPHP3)
|
ENSP00000508078.1:p.Thr456=
|
|
ENST00000337331.10:c.1660A=
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Thr554=
|
|
ENST00000337331.9:c.1660A=
(NPHP3)
|
ENSP00000338766.5:p.Thr554=
|
|
ENST00000465756.5:c.1366A=
(NPHP3)
|
ENSP00000419907.1:p.Thr456=
|
|
ENST00000469232.5:c.1475A=
(NPHP3)
|
ENSP00000418664.1:n.1475A=
|
|
ENST00000471702.2:c.1660A=
(NPHP3-ACAD11)
|
ENSP00000419763.1:p.Thr554=
|
|
ENST00000490993.5:n.1436A=
(NPHP3)
|
|
|
NM_153240.4:c.1660A=
(NPHP3)
|
NP_694972.3:p.Thr554=
|
|
NR_037804.1:n.1764A=
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.1660A=
(NPHP3)
MANE Select
|
NP_694972.3:p.Thr554=
|
|