ENST00000370192.8:c.2696A>C
(DPYD)
MANE Select
|
ENSP00000359211.3:p.Glu899Ala
|
|
ENST00000370192.7:c.2696A>C
(DPYD)
|
ENSP00000359211.3:p.Glu899Ala
|
|
NM_000110.3:c.2696A>C , LRG_722t1:c.2696A>C
(DPYD)
|
NP_000101.2:p.Glu899Ala
|
|
NR_046590.1:n.64+2573T>G
(DPYD-AS1)
|
|
|
XM_005270562.3:c.2480A>C
(DPYD)
|
XP_005270619.2:p.Glu827Ala
|
|
XM_017000507.1:c.2585A>C
(DPYD)
|
XP_016855996.1:p.Glu862Ala
|
|
XM_017000508.2:c.2201A>C
(DPYD)
|
XP_016855997.1:p.Glu734Ala
|
|
XM_017000509.2:c.2201A>C
(DPYD)
|
XP_016855998.1:p.Glu734Ala
|
|
XM_017000510.1:c.2201A>C
(DPYD)
|
XP_016855999.1:p.Glu734Ala
|
|
NM_000110.4:c.2696A>C
(DPYD)
MANE Select
|
NP_000101.2:p.Glu899Ala
|
|