ENST00000181383.10:c.1047A>G
(CPB2)
MANE Select
|
ENSP00000181383.4:p.Lys349=
|
|
ENST00000439329.5:c.936A>G
(CPB2)
|
ENSP00000400714.3:p.Lys312=
|
|
ENST00000675730.1:c.*179A>G
(CPB2)
|
ENSP00000502038.1:n.*179A>G
|
|
ENST00000181383.8:c.1047A>G
(CPB2)
|
ENSP00000181383.4:p.Lys349=
|
|
ENST00000439329.4:c.936A>G
(CPB2)
|
ENSP00000400714.3:p.Lys312=
|
|
NM_001278541.1:c.936A>G
(CPB2)
|
NP_001265470.1:p.Lys312=
|
|
NM_001872.4:c.1047A>G
(CPB2)
|
NP_001863.3:p.Lys349=
|
|
NR_046226.1:n.118+2837T>C
(CPB2-AS1)
|
|
|
NR_046227.1:n.118+2837T>C
(CPB2-AS1)
|
|
|
XM_017020393.2:c.1020A>G
(CPB2)
|
XP_016875882.1:p.Lys340=
|
|
NM_001872.5:c.1047A>G
(CPB2)
MANE Select
|
NP_001863.3:p.Lys349=
|
|
NM_001278541.2:c.936A>G
(CPB2)
|
NP_001265470.1:p.Lys312=
|
|