ENST00000357068.11:c.1678T>A
(PRODH)
MANE Select
|
ENSP00000349577.6:p.Tyr560Asn
|
|
ENST00000638240.1:c.513+2272A>T
|
ENSP00000492446.1:n.513+2272A>T
|
|
ENST00000313755.9:n.2443T>A
(PRODH)
|
|
|
ENST00000334029.6:c.1354T>A
(PRODH)
|
ENSP00000334726.2:p.Tyr452Asn
|
|
ENST00000357068.10:c.1678T>A
(PRODH)
|
ENSP00000349577.6:p.Tyr560Asn
|
|
ENST00000420436.5:c.1354T>A
(PRODH)
|
ENSP00000410805.1:p.Tyr452Asn
|
|
ENST00000429300.5:n.2049T>A
(PRODH)
|
|
|
ENST00000482858.5:n.4158T>A
(PRODH)
|
|
|
ENST00000483718.5:c.*1942A>T
(DGCR6)
|
ENSP00000467483.1:n.*1942A>T
|
|
ENST00000491604.5:n.2587T>A
(PRODH)
|
|
|
ENST00000610940.4:c.1678T>A
(PRODH)
|
ENSP00000480347.1:p.Tyr560Asn
|
|
NM_001195226.1:c.1354T>A
(PRODH)
|
NP_001182155.1:p.Tyr452Asn
|
|
NM_016335.4:c.1678T>A
(PRODH)
|
NP_057419.4:p.Tyr560Asn
|
|
XM_011530278.1:c.1105T>A
(PRODH)
|
XP_011528580.1:p.Tyr369Asn
|
|
XM_011530279.1:c.898T>A
(PRODH)
|
XP_011528581.1:p.Tyr300Asn
|
|
XR_937876.1:n.1745T>A
(PRODH)
|
|
|
NM_005675.5:c.*1611A>T
(DGCR6)
|
NP_005666.2:n.*1611A>T
|
|
NM_001195226.2:c.1354T>A
(PRODH)
|
NP_001182155.2:p.Tyr452Asn
|
|
NM_016335.5:c.1678T>A
(PRODH)
|
NP_057419.5:p.Tyr560Asn
|
|
NM_016335.6:c.1678T>A
(PRODH)
MANE Select
|
NP_057419.5:p.Tyr560Asn
|
|