ENST00000357068.11:c.1561C>T
(PRODH)
MANE Select
|
ENSP00000349577.6:p.Arg521Trp
|
|
ENST00000638240.1:c.513+2464G>A
|
ENSP00000492446.1:n.513+2464G>A
|
|
ENST00000313755.9:n.2326C>T
(PRODH)
|
|
|
ENST00000334029.6:c.1237C>T
(PRODH)
|
ENSP00000334726.2:p.Arg413Trp
|
|
ENST00000357068.10:c.1561C>T
(PRODH)
|
ENSP00000349577.6:p.Arg521Trp
|
|
ENST00000420436.5:c.1237C>T
(PRODH)
|
ENSP00000410805.1:p.Arg413Trp
|
|
ENST00000429300.5:n.1932C>T
(PRODH)
|
|
|
ENST00000482858.5:n.4041C>T
(PRODH)
|
|
|
ENST00000483718.5:c.*2134G>A
(DGCR6)
|
ENSP00000467483.1:n.*2134G>A
|
|
ENST00000491604.5:n.2470C>T
(PRODH)
|
|
|
ENST00000610940.4:c.1561C>T
(PRODH)
|
ENSP00000480347.1:p.Arg521Trp
|
|
NM_001195226.1:c.1237C>T
(PRODH)
|
NP_001182155.1:p.Gln413Ter
|
|
NM_016335.4:c.1561C>T
(PRODH)
|
NP_057419.4:p.Gln521Ter
|
|
XM_011530278.1:c.988C>T
(PRODH)
|
XP_011528580.1:p.Arg330Trp
|
|
XM_011530279.1:c.781C>T
(PRODH)
|
XP_011528581.1:p.Arg261Trp
|
|
XR_937876.1:n.1628C>T
(PRODH)
|
|
|
NM_005675.5:c.*1803G>A
(DGCR6)
|
NP_005666.2:n.*1803G>A
|
|
NM_001195226.2:c.1237C>T
(PRODH)
|
NP_001182155.2:p.Arg413Trp
|
|
NM_016335.5:c.1561C>T
(PRODH)
|
NP_057419.5:p.Arg521Trp
|
|
NM_016335.6:c.1561C>T
(PRODH)
MANE Select
|
NP_057419.5:p.Arg521Trp
|
|