ENST00000684294.1:c.1393A>G
(NPHP3)
|
ENSP00000508078.1:p.Arg465Gly
|
|
ENST00000337331.10:c.1687A>G
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Arg563Gly
|
|
ENST00000337331.9:c.1687A>G
(NPHP3)
|
ENSP00000338766.5:p.Arg563Gly
|
|
ENST00000465756.5:c.1393A>G
(NPHP3)
|
ENSP00000419907.1:p.Arg465Gly
|
|
ENST00000469232.5:c.1502A>G
(NPHP3)
|
ENSP00000418664.1:n.1502A>G
|
|
ENST00000471702.2:c.1687A>G
(NPHP3-ACAD11)
|
ENSP00000419763.1:p.Arg563Gly
|
|
ENST00000490993.5:n.1463A>G
(NPHP3)
|
|
|
NM_153240.4:c.1687A>G
(NPHP3)
|
NP_694972.3:p.Arg563Gly
|
|
NR_037804.1:n.1791A>G
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.1687A>G
(NPHP3)
MANE Select
|
NP_694972.3:p.Arg563Gly
|
|