ENST00000370192.8:c.2667C>G
(DPYD)
MANE Select
|
ENSP00000359211.3:p.Ile889Met
|
|
ENST00000370192.7:c.2667C>G
(DPYD)
|
ENSP00000359211.3:p.Ile889Met
|
|
NM_000110.3:c.2667C>G , LRG_722t1:c.2667C>G
(DPYD)
|
NP_000101.2:p.Ile889Met
|
|
NR_046590.1:n.64+2602G>C
(DPYD-AS1)
|
|
|
XM_005270562.3:c.2451C>G
(DPYD)
|
XP_005270619.2:p.Ile817Met
|
|
XM_017000507.1:c.2556C>G
(DPYD)
|
XP_016855996.1:p.Ile852Met
|
|
XM_017000508.2:c.2172C>G
(DPYD)
|
XP_016855997.1:p.Ile724Met
|
|
XM_017000509.2:c.2172C>G
(DPYD)
|
XP_016855998.1:p.Ile724Met
|
|
XM_017000510.1:c.2172C>G
(DPYD)
|
XP_016855999.1:p.Ile724Met
|
|
NM_000110.4:c.2667C>G
(DPYD)
MANE Select
|
NP_000101.2:p.Ile889Met
|
|