ENST00000406938.3:c.504C>A
(CHKB)
MANE Select
|
ENSP00000384400.3:p.Ala168=
|
|
ENST00000406938.2:c.504C>A
(CHKB)
|
ENSP00000384400.2:p.Ala168=
|
|
ENST00000463053.1:n.653C>A
(CHKB)
|
|
|
ENST00000468532.5:n.381C>A
(CHKB)
|
|
|
ENST00000476289.5:n.777C>A
(CHKB)
|
|
|
ENST00000479003.5:n.1129C>A
(CHKB)
|
|
|
ENST00000481673.5:n.954C>A
(CHKB)
|
|
|
ENST00000484266.5:n.576+752C>A
(CHKB)
|
|
|
ENST00000492556.5:n.1274C>A
(CHKB-CPT1B)
|
|
|
ENST00000492582.5:n.1163C>A
(CHKB)
|
|
|
NM_005198.4:c.504C>A , LRG_855t1:c.504C>A
(CHKB)
|
NP_005189.2:p.Ala168=
|
|
NR_027928.2:n.722C>A
(CHKB-CPT1B)
|
|
|
NM_005198.5:c.504C>A
(CHKB)
MANE Select
|
NP_005189.2:p.Ala168=
|
|