ENST00000181383.10:c.1068C>A
(CPB2)
MANE Select
|
ENSP00000181383.4:p.Gly356=
|
|
ENST00000439329.5:c.957C>A
(CPB2)
|
ENSP00000400714.3:p.Gly319=
|
|
ENST00000675730.1:c.*200C>A
(CPB2)
|
ENSP00000502038.1:n.*200C>A
|
|
ENST00000181383.8:c.1068C>A
(CPB2)
|
ENSP00000181383.4:p.Gly356=
|
|
ENST00000439329.4:c.957C>A
(CPB2)
|
ENSP00000400714.3:p.Gly319=
|
|
NM_001278541.1:c.957C>A
(CPB2)
|
NP_001265470.1:p.Gly319=
|
|
NM_001872.4:c.1068C>A
(CPB2)
|
NP_001863.3:p.Gly356=
|
|
NR_046226.1:n.118+2816G>T
(CPB2-AS1)
|
|
|
NR_046227.1:n.118+2816G>T
(CPB2-AS1)
|
|
|
XM_017020393.2:c.1041C>A
(CPB2)
|
XP_016875882.1:p.Gly347=
|
|
NM_001872.5:c.1068C>A
(CPB2)
MANE Select
|
NP_001863.3:p.Gly356=
|
|
NM_001278541.2:c.957C>A
(CPB2)
|
NP_001265470.1:p.Gly319=
|
|