ENST00000231749.8:c.567A>T
MANE Select
|
ENSP00000231749.3:p.Ser189=
|
|
ENST00000231749.7:c.567A>T
|
ENSP00000231749.3:p.Ser189=
|
|
ENST00000360165.7:c.567A>T
|
ENSP00000353289.3:p.Ser189=
|
|
ENST00000442887.1:c.438A>T
|
ENSP00000393687.1:p.Ser146=
|
|
ENST00000443080.5:c.*319A>T
|
ENSP00000415661.1:n.*319A>T
|
|
ENST00000475688.1:n.19A>T
|
|
|
NM_001308379.1:c.567A>T
|
NP_001295308.1:p.Ser189=
|
|
NM_015896.2:c.567A>T
|
NP_056980.2:p.Ser189=
|
|
NM_015896.3:c.567A>T
|
NP_056980.2:p.Ser189=
|
|
XM_005265216.2:c.330A>T
|
XP_005265273.1:p.Ser110=
|
|
XM_005265216.3:c.330A>T
|
XP_005265273.1:p.Ser110=
|
|
NM_015896.4:c.567A>T
MANE Select
|
NP_056980.2:p.Ser189=
|
|
NM_001308379.2:c.567A>T
|
NP_001295308.1:p.Ser189=
|
|