ENST00000553106.6:c.1232C=
MANE Select
|
ENSP00000448059.1:p.Ser411=
|
|
ENST00000307000.7:c.1217C=
|
ENSP00000303500.2:p.Ser406=
|
|
ENST00000551114.2:n.894C=
|
|
|
ENST00000553106.5:c.1232C=
|
ENSP00000448059.1:p.Ser411=
|
|
ENST00000635477.1:c.336C=
|
|
|
ENST00000635528.1:n.747C=
|
|
|
NM_000277.1:c.1232C=
|
NP_000268.1:p.Ser411=
|
|
XM_011538422.1:c.1175C=
|
XP_011536724.1:p.Ser392=
|
|
NM_000277.2:c.1232C=
|
NP_000268.1:p.Ser411=
|
|
NM_001354304.1:c.1232C=
|
NP_001341233.1:p.Ser411=
|
|
NM_000277.3:c.1232C=
MANE Select
|
NP_000268.1:p.Ser411=
|
|
NM_001354304.2:c.1232C=
|
NP_001341233.1:p.Ser411=
|
|