ENST00000684294.1:c.*1591C>T
(NPHP3)
|
ENSP00000508078.1:n.*1591C>T
|
|
ENST00000337331.10:c.3663C>T
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Ala1221=
|
|
ENST00000337331.9:c.3663C>T
(NPHP3)
|
ENSP00000338766.5:p.Ala1221=
|
|
ENST00000465756.5:c.*1571C>T
(NPHP3)
|
ENSP00000419907.1:n.*1571C>T
|
|
ENST00000471702.2:c.*1654C>T
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.*1654C>T
|
|
ENST00000474871.5:n.2862C>T
(NPHP3)
|
|
|
ENST00000490993.5:n.4388C>T
(NPHP3)
|
|
|
ENST00000493732.5:n.363C>T
(NPHP3)
|
|
|
ENST00000512094.5:c.225C>T
(NPHP3)
|
ENSP00000427666.1:p.Ala75=
|
|
ENST00000632629.1:c.310C>T
(NPHP3-ACAD11)
|
|
|
NM_153240.4:c.3663C>T
(NPHP3)
|
NP_694972.3:p.Ala1221=
|
|
NR_037804.1:n.3669C>T
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.3663C>T
(NPHP3)
MANE Select
|
NP_694972.3:p.Ala1221=
|
|