|
ENST00000260947.9:c.2237A>G
MANE Select
|
ENSP00000260947.4:p.His746Arg
|
|
|
ENST00000421162.2:c.884A>G
|
ENSP00000392245.2:p.His295Arg
|
|
|
ENST00000613192.2:c.*300A>G
|
ENSP00000483275.2:n.*300A>G
|
|
|
ENST00000613374.5:c.827A>G
|
ENSP00000484464.1:p.His276Arg
|
|
|
ENST00000613706.5:c.1829A>G
|
ENSP00000484976.2:p.His610Arg
|
|
|
ENST00000617164.5:c.2180A>G
|
ENSP00000480470.1:p.His727Arg
|
|
|
ENST00000619009.5:c.698A>G
|
ENSP00000482293.1:p.His233Arg
|
|
|
ENST00000650978.1:c.3612A>G
|
|
|
|
ENST00000260947.8:c.2237A>G
|
ENSP00000260947.4:p.His746Arg
|
|
|
ENST00000432456.5:c.380A>G
|
|
|
|
ENST00000455743.5:c.*1857A>G
|
ENSP00000412186.1:n.*1857A>G
|
|
|
ENST00000471590.5:n.572A>G
|
|
|
|
ENST00000613192.1:c.407A>G
|
ENSP00000483275.1:p.His136Arg
|
|
|
ENST00000613374.4:c.827A>G
|
ENSP00000484464.1:p.His276Arg
|
|
|
ENST00000613706.4:c.884A>G
|
ENSP00000484976.1:p.His295Arg
|
|
|
ENST00000617164.4:c.2180A>G
|
ENSP00000480470.1:p.His727Arg
|
|
|
ENST00000619009.4:c.698A>G
|
ENSP00000482293.1:p.His233Arg
|
|
|
ENST00000620057.4:c.*903A>G
|
ENSP00000481988.1:n.*903A>G
|
|
|
NM_000465.3:c.2237A>G
|
NP_000456.2:p.His746Arg
|
|
|
NM_001282543.1:c.2180A>G
|
NP_001269472.1:p.His727Arg
|
|
|
NM_001282545.1:c.884A>G
|
NP_001269474.1:p.His295Arg
|
|
|
NM_001282548.1:c.827A>G
|
NP_001269477.1:p.His276Arg
|
|
|
NM_001282549.1:c.698A>G
|
NP_001269478.1:p.His233Arg
|
|
|
NR_104212.1:n.2230A>G
|
|
|
|
NR_104215.1:n.2173A>G
|
|
|
|
NR_104216.1:n.1429A>G
|
|
|
|
XM_011511567.1:c.2183A>G
|
XP_011509869.1:p.His728Arg
|
|
|
XM_017004613.1:c.2336A>G
|
XP_016860102.1:p.His779Arg
|
|
|
XR_002959322.1:n.2603A>G
|
|
|
|
NM_000465.4:c.2237A>G
MANE Select
|
NP_000456.2:p.His746Arg
|
|
|
NM_001282543.2:c.2180A>G
|
NP_001269472.1:p.His727Arg
|
|
|
NM_001282545.2:c.884A>G
|
NP_001269474.1:p.His295Arg
|
|
|
NM_001282548.2:c.827A>G
|
NP_001269477.1:p.His276Arg
|
|
|
NM_001282549.2:c.698A>G
|
NP_001269478.1:p.His233Arg
|
|
|
NR_104212.2:n.2202A>G
|
|
|
|
NR_104215.2:n.2145A>G
|
|
|
|
NR_104216.2:n.1401A>G
|
|
|
