ENST00000296684.10:c.255T>C
MANE Select
|
ENSP00000296684.5:p.Asn85=
|
|
ENST00000296684.9:c.255T>C
|
ENSP00000296684.5:p.Asn85=
|
|
ENST00000502423.5:c.*122T>C
|
ENSP00000422177.1:n.*122T>C
|
|
ENST00000506765.1:c.243T>C
|
ENSP00000424570.1:p.Asn81=
|
|
ENST00000506974.5:c.*31T>C
|
ENSP00000425967.1:n.*31T>C
|
|
ENST00000507026.5:c.*229T>C
|
ENSP00000424993.1:n.*229T>C
|
|
ENST00000509443.1:n.116T>C
|
|
|
NM_002495.2:c.255T>C
|
NP_002486.1:p.Asn85=
|
|
XM_005248525.3:c.255T>C
|
XP_005248582.1:p.Asn85=
|
|
XM_011543415.1:c.81T>C
|
XP_011541717.1:p.Asn27=
|
|
NM_001318051.1:c.255T>C
|
NP_001304980.1:p.Asn85=
|
|
NM_002495.3:c.255T>C
|
NP_002486.1:p.Asn85=
|
|
NR_134473.1:n.457T>C
|
|
|
NR_134474.1:n.374T>C
|
|
|
NR_134475.1:n.409T>C
|
|
|
NM_002495.4:c.255T>C
MANE Select
|
NP_002486.1:p.Asn85=
|
|
NM_001318051.2:c.255T>C
|
NP_001304980.1:p.Asn85=
|
|
NR_134473.2:n.451T>C
|
|
|
NR_134474.2:n.368T>C
|
|
|
NR_134475.2:n.403T>C
|
|
|