ENST00000573725.2:c.6795T>C
|
ENSP00000460849.2:p.Val2265=
|
|
ENST00000703537.1:c.2723T>C
|
|
|
ENST00000703538.1:c.*6698T>C
|
ENSP00000515361.1:n.*6698T>C
|
|
ENST00000703539.1:n.3289T>C
|
|
|
ENST00000703540.1:c.6828T>C
|
ENSP00000515362.1:p.Val2276=
|
|
ENST00000703541.1:c.6840T>C
|
ENSP00000515363.1:p.Val2280=
|
|
ENST00000304992.11:c.6975T>C
MANE Select
|
ENSP00000304350.6:p.Val2325=
|
|
ENST00000304992.10:c.6975T>C
|
ENSP00000304350.6:p.Val2325=
|
|
ENST00000571958.1:c.174T>C
|
|
|
ENST00000572621.5:c.6975T>C
|
ENSP00000460348.1:p.Val2325=
|
|
NM_006445.3:c.6975T>C
|
NP_006436.3:p.Val2325=
|
|
XM_024450537.1:c.6975T>C
|
XP_024306305.1:p.Val2325=
|
|
NM_006445.4:c.6975T>C
MANE Select
|
NP_006436.3:p.Val2325=
|
|