ENST00000370192.8:c.2291G>A
(DPYD)
MANE Select
|
ENSP00000359211.3:p.Gly764Glu
|
|
ENST00000370192.7:c.2291G>A
(DPYD)
|
ENSP00000359211.3:p.Gly764Glu
|
|
NM_000110.3:c.2291G>A , LRG_722t1:c.2291G>A
(DPYD)
|
NP_000101.2:p.Gly764Glu
|
|
NR_046590.1:n.129-922C>T
(DPYD-AS1)
|
|
|
XM_005270562.3:c.2075G>A
(DPYD)
|
XP_005270619.2:p.Gly692Glu
|
|
XM_006710397.2:c.2291G>A
(DPYD)
|
XP_006710460.1:p.Gly764Glu
|
|
XM_006710397.3:c.2291G>A
(DPYD)
|
XP_006710460.1:p.Gly764Glu
|
|
XM_017000507.1:c.2180G>A
(DPYD)
|
XP_016855996.1:p.Gly727Glu
|
|
XM_017000508.2:c.1796G>A
(DPYD)
|
XP_016855997.1:p.Gly599Glu
|
|
XM_017000509.2:c.1796G>A
(DPYD)
|
XP_016855998.1:p.Gly599Glu
|
|
XM_017000510.1:c.1796G>A
(DPYD)
|
XP_016855999.1:p.Gly599Glu
|
|
NM_000110.4:c.2291G>A
(DPYD)
MANE Select
|
NP_000101.2:p.Gly764Glu
|
|