ENST00000370192.8:c.2591C=
(DPYD)
MANE Select
|
ENSP00000359211.3:p.Pro864=
|
|
ENST00000370192.7:c.2591C=
(DPYD)
|
ENSP00000359211.3:p.Pro864=
|
|
NM_000110.3:c.2591C= , LRG_722t1:c.2591C=
(DPYD)
|
NP_000101.2:p.Pro864=
|
|
NR_046590.1:n.65-72314G=
(DPYD-AS1)
|
|
|
XM_005270562.3:c.2375C=
(DPYD)
|
XP_005270619.2:p.Pro792=
|
|
XM_006710397.2:c.2591C=
(DPYD)
|
XP_006710460.1:p.Pro864=
|
|
XM_006710397.3:c.2591C=
(DPYD)
|
XP_006710460.1:p.Pro864=
|
|
XM_017000507.1:c.2480C=
(DPYD)
|
XP_016855996.1:p.Pro827=
|
|
XM_017000508.2:c.2096C=
(DPYD)
|
XP_016855997.1:p.Pro699=
|
|
XM_017000509.2:c.2096C=
(DPYD)
|
XP_016855998.1:p.Pro699=
|
|
XM_017000510.1:c.2096C=
(DPYD)
|
XP_016855999.1:p.Pro699=
|
|
NM_000110.4:c.2591C=
(DPYD)
MANE Select
|
NP_000101.2:p.Pro864=
|
|