ENST00000296684.10:c.406T>C
MANE Select
|
ENSP00000296684.5:p.Ser136Pro
|
|
ENST00000296684.9:c.406T>C
|
ENSP00000296684.5:p.Ser136Pro
|
|
ENST00000502423.5:c.*273T>C
|
ENSP00000422177.1:n.*273T>C
|
|
ENST00000506765.1:c.338+12201T>C
|
ENSP00000424570.1:n.338+12201T>C
|
|
ENST00000506974.5:c.*182T>C
|
ENSP00000425967.1:n.*182T>C
|
|
ENST00000507026.5:c.*380T>C
|
ENSP00000424993.1:n.*380T>C
|
|
ENST00000509443.1:n.267T>C
|
|
|
NM_002495.2:c.406T>C
|
NP_002486.1:p.Ser136Pro
|
|
XM_005248525.3:c.350+12201T>C
|
XP_005248582.1:n.350+12201T>C
|
|
XM_011543415.1:c.232T>C
|
XP_011541717.1:p.Ser78Pro
|
|
NM_001318051.1:c.350+12201T>C
|
NP_001304980.1:n.350+12201T>C
|
|
NM_002495.3:c.406T>C
|
NP_002486.1:p.Ser136Pro
|
|
NR_134473.1:n.608T>C
|
|
|
NR_134474.1:n.525T>C
|
|
|
NR_134475.1:n.560T>C
|
|
|
NM_002495.4:c.406T>C
MANE Select
|
NP_002486.1:p.Ser136Pro
|
|
NM_001318051.2:c.350+12201T>C
|
NP_001304980.1:n.350+12201T>C
|
|
NR_134473.2:n.602T>C
|
|
|
NR_134474.2:n.519T>C
|
|
|
NR_134475.2:n.554T>C
|
|
|