ENST00000370192.8:c.2736T>C
(DPYD)
MANE Select
|
ENSP00000359211.3:p.Phe912=
|
|
ENST00000370192.7:c.2736T>C
(DPYD)
|
ENSP00000359211.3:p.Phe912=
|
|
NM_000110.3:c.2736T>C , LRG_722t1:c.2736T>C
(DPYD)
|
NP_000101.2:p.Phe912=
|
|
NR_046590.1:n.64+2533A>G
(DPYD-AS1)
|
|
|
XM_005270562.3:c.2520T>C
(DPYD)
|
XP_005270619.2:p.Phe840=
|
|
XM_017000507.1:c.2625T>C
(DPYD)
|
XP_016855996.1:p.Phe875=
|
|
XM_017000508.2:c.2241T>C
(DPYD)
|
XP_016855997.1:p.Phe747=
|
|
XM_017000509.2:c.2241T>C
(DPYD)
|
XP_016855998.1:p.Phe747=
|
|
XM_017000510.1:c.2241T>C
(DPYD)
|
XP_016855999.1:p.Phe747=
|
|
NM_000110.4:c.2736T>C
(DPYD)
MANE Select
|
NP_000101.2:p.Phe912=
|
|