ENST00000357068.11:c.1668G>C
(PRODH)
MANE Select
|
ENSP00000349577.6:p.Glu556Asp
|
|
ENST00000638240.1:c.513+2282C>G
|
ENSP00000492446.1:n.513+2282C>G
|
|
ENST00000313755.9:n.2433G>C
(PRODH)
|
|
|
ENST00000334029.6:c.1344G>C
(PRODH)
|
ENSP00000334726.2:p.Glu448Asp
|
|
ENST00000357068.10:c.1668G>C
(PRODH)
|
ENSP00000349577.6:p.Glu556Asp
|
|
ENST00000420436.5:c.1344G>C
(PRODH)
|
ENSP00000410805.1:p.Glu448Asp
|
|
ENST00000429300.5:n.2039G>C
(PRODH)
|
|
|
ENST00000482858.5:n.4148G>C
(PRODH)
|
|
|
ENST00000483718.5:c.*1952C>G
(DGCR6)
|
ENSP00000467483.1:n.*1952C>G
|
|
ENST00000491604.5:n.2577G>C
(PRODH)
|
|
|
ENST00000610940.4:c.1668G>C
(PRODH)
|
ENSP00000480347.1:p.Glu556Asp
|
|
NM_001195226.1:c.1344G>C
(PRODH)
|
NP_001182155.1:p.Glu448Asp
|
|
NM_016335.4:c.1668G>C
(PRODH)
|
NP_057419.4:p.Glu556Asp
|
|
XM_011530278.1:c.1095G>C
(PRODH)
|
XP_011528580.1:p.Glu365Asp
|
|
XM_011530279.1:c.888G>C
(PRODH)
|
XP_011528581.1:p.Glu296Asp
|
|
XR_937876.1:n.1735G>C
(PRODH)
|
|
|
NM_005675.5:c.*1621C>G
(DGCR6)
|
NP_005666.2:n.*1621C>G
|
|
NM_001195226.2:c.1344G>C
(PRODH)
|
NP_001182155.2:p.Glu448Asp
|
|
NM_016335.5:c.1668G>C
(PRODH)
|
NP_057419.5:p.Glu556Asp
|
|
NM_016335.6:c.1668G>C
(PRODH)
MANE Select
|
NP_057419.5:p.Glu556Asp
|
|