ENST00000357068.11:c.1591T>C
(PRODH)
MANE Select
|
ENSP00000349577.6:p.Cys531Arg
|
|
ENST00000638240.1:c.513+2434A>G
|
ENSP00000492446.1:n.513+2434A>G
|
|
ENST00000313755.9:n.2356T>C
(PRODH)
|
|
|
ENST00000334029.6:c.1267T>C
(PRODH)
|
ENSP00000334726.2:p.Cys423Arg
|
|
ENST00000357068.10:c.1591T>C
(PRODH)
|
ENSP00000349577.6:p.Cys531Arg
|
|
ENST00000420436.5:c.1267T>C
(PRODH)
|
ENSP00000410805.1:p.Cys423Arg
|
|
ENST00000429300.5:n.1962T>C
(PRODH)
|
|
|
ENST00000482858.5:n.4071T>C
(PRODH)
|
|
|
ENST00000483718.5:c.*2104A>G
(DGCR6)
|
ENSP00000467483.1:n.*2104A>G
|
|
ENST00000491604.5:n.2500T>C
(PRODH)
|
|
|
ENST00000610940.4:c.1591T>C
(PRODH)
|
ENSP00000480347.1:p.Cys531Arg
|
|
NM_001195226.1:c.1267T>C
(PRODH)
|
NP_001182155.1:p.Cys423Arg
|
|
NM_016335.4:c.1591T>C
(PRODH)
|
NP_057419.4:p.Cys531Arg
|
|
XM_011530278.1:c.1018T>C
(PRODH)
|
XP_011528580.1:p.Cys340Arg
|
|
XM_011530279.1:c.811T>C
(PRODH)
|
XP_011528581.1:p.Cys271Arg
|
|
XR_937876.1:n.1658T>C
(PRODH)
|
|
|
NM_005675.5:c.*1773A>G
(DGCR6)
|
NP_005666.2:n.*1773A>G
|
|
NM_001195226.2:c.1267T>C
(PRODH)
|
NP_001182155.2:p.Cys423Arg
|
|
NM_016335.5:c.1591T>C
(PRODH)
|
NP_057419.5:p.Cys531Arg
|
|
NM_016335.6:c.1591T>C
(PRODH)
MANE Select
|
NP_057419.5:p.Cys531Arg
|
|