ENST00000296684.10:c.397G>C
MANE Select
|
ENSP00000296684.5:p.Asp133His
|
|
ENST00000296684.9:c.397G>C
|
ENSP00000296684.5:p.Asp133His
|
|
ENST00000502423.5:c.*264G>C
|
ENSP00000422177.1:n.*264G>C
|
|
ENST00000506765.1:c.338+12192G>C
|
ENSP00000424570.1:n.338+12192G>C
|
|
ENST00000506974.5:c.*173G>C
|
ENSP00000425967.1:n.*173G>C
|
|
ENST00000507026.5:c.*371G>C
|
ENSP00000424993.1:n.*371G>C
|
|
ENST00000509443.1:n.258G>C
|
|
|
NM_002495.2:c.397G>C
|
NP_002486.1:p.Asp133His
|
|
XM_005248525.3:c.350+12192G>C
|
XP_005248582.1:n.350+12192G>C
|
|
XM_011543415.1:c.223G>C
|
XP_011541717.1:p.Asp75His
|
|
NM_001318051.1:c.350+12192G>C
|
NP_001304980.1:n.350+12192G>C
|
|
NM_002495.3:c.397G>C
|
NP_002486.1:p.Asp133His
|
|
NR_134473.1:n.599G>C
|
|
|
NR_134474.1:n.516G>C
|
|
|
NR_134475.1:n.551G>C
|
|
|
NM_002495.4:c.397G>C
MANE Select
|
NP_002486.1:p.Asp133His
|
|
NM_001318051.2:c.350+12192G>C
|
NP_001304980.1:n.350+12192G>C
|
|
NR_134473.2:n.593G>C
|
|
|
NR_134474.2:n.510G>C
|
|
|
NR_134475.2:n.545G>C
|
|
|