ENST00000357068.11:c.1757T=
(PRODH)
MANE Select
|
ENSP00000349577.6:p.Leu586=
|
|
ENST00000638240.1:c.513+2193A=
|
ENSP00000492446.1:n.513+2193A=
|
|
ENST00000313755.9:n.2522T=
(PRODH)
|
|
|
ENST00000334029.6:c.1433T=
(PRODH)
|
ENSP00000334726.2:p.Leu478=
|
|
ENST00000357068.10:c.1757T=
(PRODH)
|
ENSP00000349577.6:p.Leu586=
|
|
ENST00000420436.5:c.1433T=
(PRODH)
|
ENSP00000410805.1:p.Leu478=
|
|
ENST00000429300.5:n.2128T=
(PRODH)
|
|
|
ENST00000482858.5:n.4237T=
(PRODH)
|
|
|
ENST00000483718.5:c.*1863A=
(DGCR6)
|
ENSP00000467483.1:n.*1863A=
|
|
ENST00000491604.5:n.2666T=
(PRODH)
|
|
|
ENST00000610940.4:c.1757T=
(PRODH)
|
ENSP00000480347.1:p.Leu586=
|
|
NM_001195226.1:c.1433T=
(PRODH)
|
NP_001182155.1:p.Leu478=
|
|
NM_016335.4:c.1757T=
(PRODH)
|
NP_057419.4:p.Leu586=
|
|
XM_011530278.1:c.1184T=
(PRODH)
|
XP_011528580.1:p.Leu395=
|
|
XM_011530279.1:c.977T=
(PRODH)
|
XP_011528581.1:p.Leu326=
|
|
XR_937876.1:n.1824T=
(PRODH)
|
|
|
NM_005675.5:c.*1532A=
(DGCR6)
|
NP_005666.2:n.*1532A=
|
|
NM_001195226.2:c.1433T=
(PRODH)
|
NP_001182155.2:p.Leu478=
|
|
NM_016335.5:c.1757T=
(PRODH)
|
NP_057419.5:p.Leu586=
|
|
NM_016335.6:c.1757T=
(PRODH)
MANE Select
|
NP_057419.5:p.Leu586=
|
|