ENST00000573725.2:c.6534C=
|
ENSP00000460849.2:p.Gly2178=
|
|
ENST00000703537.1:c.2462C=
|
|
|
ENST00000703538.1:c.*6437C=
|
ENSP00000515361.1:n.*6437C=
|
|
ENST00000703539.1:n.3028C=
|
|
|
ENST00000703540.1:c.6567C=
|
ENSP00000515362.1:p.Gly2189=
|
|
ENST00000703541.1:c.6579C=
|
ENSP00000515363.1:p.Gly2193=
|
|
ENST00000304992.11:c.6714C=
MANE Select
|
ENSP00000304350.6:p.Gly2238=
|
|
ENST00000304992.10:c.6714C=
|
ENSP00000304350.6:p.Gly2238=
|
|
ENST00000571958.1:c.23C=
|
|
|
ENST00000572621.5:c.6714C=
|
ENSP00000460348.1:p.Gly2238=
|
|
ENST00000572723.1:n.703C=
|
|
|
NM_006445.3:c.6714C=
|
NP_006436.3:p.Gly2238=
|
|
XM_024450537.1:c.6714C=
|
XP_024306305.1:p.Gly2238=
|
|
NM_006445.4:c.6714C=
MANE Select
|
NP_006436.3:p.Gly2238=
|
|