ENST00000296684.10:c.300G>T
MANE Select
|
ENSP00000296684.5:p.Glu100Asp
|
|
ENST00000296684.9:c.300G>T
|
ENSP00000296684.5:p.Glu100Asp
|
|
ENST00000502423.5:c.*167G>T
|
ENSP00000422177.1:n.*167G>T
|
|
ENST00000506765.1:c.288G>T
|
ENSP00000424570.1:p.Glu96Asp
|
|
ENST00000506974.5:c.*76G>T
|
ENSP00000425967.1:n.*76G>T
|
|
ENST00000507026.5:c.*274G>T
|
ENSP00000424993.1:n.*274G>T
|
|
ENST00000509443.1:n.161G>T
|
|
|
NM_002495.2:c.300G>T
|
NP_002486.1:p.Glu100Asp
|
|
XM_005248525.3:c.300G>T
|
XP_005248582.1:p.Glu100Asp
|
|
XM_011543415.1:c.126G>T
|
XP_011541717.1:p.Glu42Asp
|
|
NM_001318051.1:c.300G>T
|
NP_001304980.1:p.Glu100Asp
|
|
NM_002495.3:c.300G>T
|
NP_002486.1:p.Glu100Asp
|
|
NR_134473.1:n.502G>T
|
|
|
NR_134474.1:n.419G>T
|
|
|
NR_134475.1:n.454G>T
|
|
|
NM_002495.4:c.300G>T
MANE Select
|
NP_002486.1:p.Glu100Asp
|
|
NM_001318051.2:c.300G>T
|
NP_001304980.1:p.Glu100Asp
|
|
NR_134473.2:n.496G>T
|
|
|
NR_134474.2:n.413G>T
|
|
|
NR_134475.2:n.448G>T
|
|
|