ENST00000406938.3:c.207G>T
(CHKB)
MANE Select
|
ENSP00000384400.3:p.Leu69=
|
|
ENST00000406938.2:c.207G>T
(CHKB)
|
ENSP00000384400.2:p.Leu69=
|
|
ENST00000463053.1:n.307-218G>T
(CHKB)
|
|
|
ENST00000476289.5:n.280G>T
(CHKB)
|
|
|
ENST00000479003.5:n.246G>T
(CHKB)
|
|
|
ENST00000481673.5:n.271G>T
(CHKB)
|
|
|
ENST00000484266.5:n.250G>T
(CHKB)
|
|
|
ENST00000492556.5:n.391G>T
(CHKB-CPT1B)
|
|
|
ENST00000492582.5:n.280G>T
(CHKB)
|
|
|
NM_005198.4:c.207G>T , LRG_855t1:c.207G>T
(CHKB)
|
NP_005189.2:p.Leu69=
|
|
NR_027928.2:n.425G>T
(CHKB-CPT1B)
|
|
|
NM_005198.5:c.207G>T
(CHKB)
MANE Select
|
NP_005189.2:p.Leu69=
|
|