ENST00000573725.2:c.6519T=
|
ENSP00000460849.2:p.Ser2173=
|
|
ENST00000703537.1:c.2447T=
|
|
|
ENST00000703538.1:c.*6422T=
|
ENSP00000515361.1:n.*6422T=
|
|
ENST00000703539.1:n.3013T=
|
|
|
ENST00000703540.1:c.6552T=
|
ENSP00000515362.1:p.Ser2184=
|
|
ENST00000703541.1:c.6564T=
|
ENSP00000515363.1:p.Ser2188=
|
|
ENST00000304992.11:c.6699T=
MANE Select
|
ENSP00000304350.6:p.Ser2233=
|
|
ENST00000304992.10:c.6699T=
|
ENSP00000304350.6:p.Ser2233=
|
|
ENST00000571958.1:c.8T=
|
|
|
ENST00000572621.5:c.6699T=
|
ENSP00000460348.1:p.Ser2233=
|
|
ENST00000572723.1:n.688T=
|
|
|
NM_006445.3:c.6699T=
|
NP_006436.3:p.Ser2233=
|
|
XM_024450537.1:c.6699T=
|
XP_024306305.1:p.Ser2233=
|
|
NM_006445.4:c.6699T=
MANE Select
|
NP_006436.3:p.Ser2233=
|
|