ENST00000684294.1:c.*706G>A
(NPHP3)
|
ENSP00000508078.1:n.*706G>A
|
|
ENST00000337331.10:c.2798G>A
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Cys933Tyr
|
|
ENST00000337331.9:c.2798G>A
(NPHP3)
|
ENSP00000338766.5:p.Cys933Tyr
|
|
ENST00000465756.5:c.*706G>A
(NPHP3)
|
ENSP00000419907.1:n.*706G>A
|
|
ENST00000471702.2:c.*789G>A
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.*789G>A
|
|
ENST00000474871.5:n.532G>A
(NPHP3)
|
|
|
ENST00000490993.5:n.3523G>A
(NPHP3)
|
|
|
NM_153240.4:c.2798G>A
(NPHP3)
|
NP_694972.3:p.Cys933Tyr
|
|
NR_037804.1:n.2804G>A
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.2798G>A
(NPHP3)
MANE Select
|
NP_694972.3:p.Cys933Tyr
|
|