|
ENST00000444124.7:c.882A>C
(DDC)
MANE Select
|
ENSP00000403644.2:p.Ala294=
|
|
|
ENST00000357936.9:c.882A>C
(DDC)
|
ENSP00000350616.5:p.Ala294=
|
|
|
ENST00000380984.4:c.882A>C
(DDC)
|
ENSP00000370371.4:p.Ala294=
|
|
|
ENST00000426377.5:c.648A>C
(DDC)
|
ENSP00000395069.1:p.Ala216=
|
|
|
ENST00000430300.5:c.524A>C
(DDC)
|
|
|
|
ENST00000431062.5:c.603A>C
(DDC)
|
ENSP00000399184.1:p.Ala201=
|
|
|
ENST00000444124.6:c.882A>C
(DDC)
|
ENSP00000403644.2:p.Ala294=
|
|
|
ENST00000444733.5:c.673A>C
(DDC)
|
ENSP00000393724.1:p.Arg225=
|
|
|
ENST00000613602.3:c.-11+47106A>C
(FIGNL1)
|
ENSP00000481751.1:n.-11+47106A>C
|
|
|
ENST00000615193.4:c.603A>C
(DDC)
|
ENSP00000484104.1:p.Ala201=
|
|
|
ENST00000617822.4:c.738A>C
(DDC)
|
ENSP00000478385.1:p.Ala246=
|
|
|
ENST00000622873.4:c.768A>C
(DDC)
|
ENSP00000479110.1:p.Ala256=
|
|
|
NM_000790.3:c.882A>C
(DDC)
|
NP_000781.1:p.Ala294=
|
|
|
NM_001082971.1:c.882A>C
(DDC)
|
NP_001076440.1:p.Ala294=
|
|
|
NM_001242886.1:c.768A>C
(DDC)
|
NP_001229815.1:p.Ala256=
|
|
|
NM_001242887.1:c.738A>C
(DDC)
|
NP_001229816.1:p.Ala246=
|
|
|
NM_001242888.1:c.648A>C
(DDC)
|
NP_001229817.1:p.Ala216=
|
|
|
NM_001242889.1:c.603A>C
(DDC)
|
NP_001229818.1:p.Ala201=
|
|
|
NM_001242890.1:c.882A>C
(DDC)
|
NP_001229819.1:p.Ala294=
|
|
|
XM_005271745.3:c.768A>C
(DDC)
|
XP_005271802.1:p.Ala256=
|
|
|
XM_011515161.1:c.531A>C
(DDC)
|
XP_011513463.1:p.Ala177=
|
|
|
XM_005271745.4:c.768A>C
(DDC)
|
XP_005271802.1:p.Ala256=
|
|
|
XM_011515161.2:c.825A>C
(DDC)
|
XP_011513463.2:p.Ala275=
|
|
|
NM_001082971.2:c.882A>C
(DDC)
MANE Select
|
NP_001076440.2:p.Ala294=
|
|
|
NM_000790.4:c.882A>C
(DDC)
|
NP_000781.2:p.Ala294=
|
|
|
NM_001242888.2:c.648A>C
(DDC)
|
NP_001229817.2:p.Ala216=
|
|
|
NM_001242890.2:c.882A>C
(DDC)
|
NP_001229819.2:p.Ala294=
|
|
|
NM_001242886.2:c.768A>C
(DDC)
|
NP_001229815.2:p.Ala256=
|
|
|
NM_001242887.2:c.738A>C
(DDC)
|
NP_001229816.2:p.Ala246=
|
|
|
NM_001242889.2:c.603A>C
(DDC)
|
NP_001229818.2:p.Ala201=
|
|
