ENST00000406938.3:c.513G>T
(CHKB)
MANE Select
|
ENSP00000384400.3:p.Met171Ile
|
|
ENST00000406938.2:c.513G>T
(CHKB)
|
ENSP00000384400.2:p.Met171Ile
|
|
ENST00000463053.1:n.662G>T
(CHKB)
|
|
|
ENST00000468532.5:n.390G>T
(CHKB)
|
|
|
ENST00000476289.5:n.786G>T
(CHKB)
|
|
|
ENST00000479003.5:n.1138G>T
(CHKB)
|
|
|
ENST00000481673.5:n.963G>T
(CHKB)
|
|
|
ENST00000484266.5:n.576+761G>T
(CHKB)
|
|
|
ENST00000492556.5:n.1283G>T
(CHKB-CPT1B)
|
|
|
ENST00000492582.5:n.1172G>T
(CHKB)
|
|
|
NM_005198.4:c.513G>T , LRG_855t1:c.513G>T
(CHKB)
|
NP_005189.2:p.Met171Ile
|
|
NR_027928.2:n.731G>T
(CHKB-CPT1B)
|
|
|
NM_005198.5:c.513G>T
(CHKB)
MANE Select
|
NP_005189.2:p.Met171Ile
|
|