ENST00000684294.1:c.*791G>T
(NPHP3)
|
ENSP00000508078.1:n.*791G>T
|
|
ENST00000337331.10:c.2883G>T
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Gln961His
|
|
ENST00000337331.9:c.2883G>T
(NPHP3)
|
ENSP00000338766.5:p.Gln961His
|
|
ENST00000465756.5:c.*791G>T
(NPHP3)
|
ENSP00000419907.1:n.*791G>T
|
|
ENST00000471702.2:c.*874G>T
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.*874G>T
|
|
ENST00000474871.5:n.617G>T
(NPHP3)
|
|
|
ENST00000490993.5:n.3608G>T
(NPHP3)
|
|
|
NM_153240.4:c.2883G>T
(NPHP3)
|
NP_694972.3:p.Gln961His
|
|
NR_037804.1:n.2889G>T
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.2883G>T
(NPHP3)
MANE Select
|
NP_694972.3:p.Gln961His
|
|