ENST00000684294.1:c.1343T>G
(NPHP3)
|
ENSP00000508078.1:p.Leu448Ter
|
|
ENST00000337331.10:c.1637T>G
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Leu546Ter
|
|
ENST00000337331.9:c.1637T>G
(NPHP3)
|
ENSP00000338766.5:p.Leu546Ter
|
|
ENST00000465756.5:c.1343T>G
(NPHP3)
|
ENSP00000419907.1:p.Leu448Ter
|
|
ENST00000469232.5:c.1452T>G
(NPHP3)
|
ENSP00000418664.1:n.1452T>G
|
|
ENST00000471702.2:c.1637T>G
(NPHP3-ACAD11)
|
ENSP00000419763.1:p.Leu546Ter
|
|
ENST00000490993.5:n.1413T>G
(NPHP3)
|
|
|
NM_153240.4:c.1637T>G
(NPHP3)
|
NP_694972.3:p.Leu546Ter
|
|
NR_037804.1:n.1741T>G
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.1637T>G
(NPHP3)
MANE Select
|
NP_694972.3:p.Leu546Ter
|
|