ENST00000296684.10:c.408C>T
MANE Select
|
ENSP00000296684.5:p.Ser136=
|
|
ENST00000296684.9:c.408C>T
|
ENSP00000296684.5:p.Ser136=
|
|
ENST00000502423.5:c.*275C>T
|
ENSP00000422177.1:n.*275C>T
|
|
ENST00000506765.1:c.338+12203C>T
|
ENSP00000424570.1:n.338+12203C>T
|
|
ENST00000506974.5:c.*184C>T
|
ENSP00000425967.1:n.*184C>T
|
|
ENST00000507026.5:c.*382C>T
|
ENSP00000424993.1:n.*382C>T
|
|
ENST00000509443.1:n.269C>T
|
|
|
NM_002495.2:c.408C>T
|
NP_002486.1:p.Ser136=
|
|
XM_005248525.3:c.350+12203C>T
|
XP_005248582.1:n.350+12203C>T
|
|
XM_011543415.1:c.234C>T
|
XP_011541717.1:p.Ser78=
|
|
NM_001318051.1:c.350+12203C>T
|
NP_001304980.1:n.350+12203C>T
|
|
NM_002495.3:c.408C>T
|
NP_002486.1:p.Ser136=
|
|
NR_134473.1:n.610C>T
|
|
|
NR_134474.1:n.527C>T
|
|
|
NR_134475.1:n.562C>T
|
|
|
NM_002495.4:c.408C>T
MANE Select
|
NP_002486.1:p.Ser136=
|
|
NM_001318051.2:c.350+12203C>T
|
NP_001304980.1:n.350+12203C>T
|
|
NR_134473.2:n.604C>T
|
|
|
NR_134474.2:n.521C>T
|
|
|
NR_134475.2:n.556C>T
|
|
|