ENST00000573725.2:c.6501C>T
|
ENSP00000460849.2:p.Ala2167=
|
|
ENST00000703537.1:c.2429C>T
|
|
|
ENST00000703538.1:c.*6404C>T
|
ENSP00000515361.1:n.*6404C>T
|
|
ENST00000703539.1:n.2995C>T
|
|
|
ENST00000703540.1:c.6534C>T
|
ENSP00000515362.1:p.Ala2178=
|
|
ENST00000703541.1:c.6546C>T
|
ENSP00000515363.1:p.Ala2182=
|
|
ENST00000304992.11:c.6681C>T
MANE Select
|
ENSP00000304350.6:p.Ala2227=
|
|
ENST00000304992.10:c.6681C>T
|
ENSP00000304350.6:p.Ala2227=
|
|
ENST00000572621.5:c.6681C>T
|
ENSP00000460348.1:p.Ala2227=
|
|
ENST00000572723.1:n.670C>T
|
|
|
NM_006445.3:c.6681C>T
|
NP_006436.3:p.Ala2227=
|
|
XM_024450537.1:c.6681C>T
|
XP_024306305.1:p.Ala2227=
|
|
NM_006445.4:c.6681C>T
MANE Select
|
NP_006436.3:p.Ala2227=
|
|