ENST00000370192.8:c.2746_2747delinsAG
(DPYD)
MANE Select
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ENSP00000359211.3:p.Arg916=
|
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ENST00000370192.7:c.2746_2747delinsAG
(DPYD)
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ENSP00000359211.3:p.Arg916=
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NM_000110.3:c.2746_2747delinsAG , LRG_722t1:c.2746_2747delinsAG
(DPYD)
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NP_000101.2:p.Arg916=
|
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NR_046590.1:n.64+2522_64+2523delinsCT
(DPYD-AS1)
|
|
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XM_005270562.3:c.2530_2531delinsAG
(DPYD)
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XP_005270619.2:p.Arg844=
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XM_017000507.1:c.2635_2636delinsAG
(DPYD)
|
XP_016855996.1:p.Arg879=
|
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XM_017000508.2:c.2251_2252delinsAG
(DPYD)
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XP_016855997.1:p.Arg751=
|
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XM_017000509.2:c.2251_2252delinsAG
(DPYD)
|
XP_016855998.1:p.Arg751=
|
|
XM_017000510.1:c.2251_2252delinsAG
(DPYD)
|
XP_016855999.1:p.Arg751=
|
|
NM_000110.4:c.2746_2747delinsAG
(DPYD)
MANE Select
|
NP_000101.2:p.Arg916=
|
|