ENST00000296684.10:c.323A>T
MANE Select
|
ENSP00000296684.5:p.Glu108Val
|
|
ENST00000296684.9:c.323A>T
|
ENSP00000296684.5:p.Glu108Val
|
|
ENST00000502423.5:c.*190A>T
|
ENSP00000422177.1:n.*190A>T
|
|
ENST00000506765.1:c.311A>T
|
ENSP00000424570.1:p.Glu104Val
|
|
ENST00000506974.5:c.*99A>T
|
ENSP00000425967.1:n.*99A>T
|
|
ENST00000507026.5:c.*297A>T
|
ENSP00000424993.1:n.*297A>T
|
|
ENST00000509443.1:n.184A>T
|
|
|
NM_002495.2:c.323A>T
|
NP_002486.1:p.Glu108Val
|
|
XM_005248525.3:c.323A>T
|
XP_005248582.1:p.Glu108Val
|
|
XM_011543415.1:c.149A>T
|
XP_011541717.1:p.Glu50Val
|
|
NM_001318051.1:c.323A>T
|
NP_001304980.1:p.Glu108Val
|
|
NM_002495.3:c.323A>T
|
NP_002486.1:p.Glu108Val
|
|
NR_134473.1:n.525A>T
|
|
|
NR_134474.1:n.442A>T
|
|
|
NR_134475.1:n.477A>T
|
|
|
NM_002495.4:c.323A>T
MANE Select
|
NP_002486.1:p.Glu108Val
|
|
NM_001318051.2:c.323A>T
|
NP_001304980.1:p.Glu108Val
|
|
NR_134473.2:n.519A>T
|
|
|
NR_134474.2:n.436A>T
|
|
|
NR_134475.2:n.471A>T
|
|
|