|
NM_000051.4:c.2332A>T
MANE Select
|
NP_000042.3:p.Asn778Tyr
|
|
ENST00000675843.1:c.2332A>T
MANE Select
|
ENSP00000501606.1:p.Asn778Tyr
|
|
NM_000051.3:c.2332A>T , LRG_135t1:c.2332A>T
|
NP_000042.3:p.Asn778Tyr
|
|
NM_001351834.1:c.2332A>T
|
NP_001338763.1:p.Asn778Tyr
|
|
NM_001351834.2:c.2332A>T
|
NP_001338763.1:p.Asn778Tyr
|
|
ENST00000278616.8:c.2332A>T
|
ENSP00000278616.4:p.Asn778Tyr
|
|
ENST00000278616.9:c.2332A>T
|
ENSP00000278616.4:p.Asn778Tyr
|
|
ENST00000452508.6:c.2332A>T
|
ENSP00000388058.2:p.Asn778Tyr
|
|
ENST00000452508.7:c.2332A>T
|
ENSP00000388058.2:p.Asn778Tyr
|
|
ENST00000527805.5:c.2332A>T
|
ENSP00000435747.1:p.Asn778Tyr
|
|
ENST00000527805.6:c.2332A>T
|
ENSP00000435747.2:p.Asn778Tyr
|
|
ENST00000675595.1:c.2167A>T
|
ENSP00000502563.1:p.Asn723Tyr
|
|
ENST00000682516.1:n.2466A>T
|
|
|
ENST00000683174.1:n.2482A>T
|
|
|
ENST00000683605.1:n.1827A>T
|
|
|
ENST00000684037.1:c.*1267A>T
|
ENSP00000508245.1:n.*1267A>T
|
|
ENST00000713593.1:c.*1803A>T
|
ENSP00000518889.1:n.*1803A>T
|
|
XM_005271561.3:c.2332A>T
|
XP_005271618.2:p.Asn778Tyr
|
|
XM_005271562.3:c.2332A>T
|
XP_005271619.2:p.Asn778Tyr
|
|
XM_005271562.5:c.2332A>T
|
XP_005271619.2:p.Asn778Tyr
|
|
XM_006718843.2:c.2332A>T
|
XP_006718906.1:p.Asn778Tyr
|
|
XM_006718843.4:c.2332A>T
|
XP_006718906.1:p.Asn778Tyr
|
|
XM_011542840.1:c.2332A>T
|
XP_011541142.1:p.Asn778Tyr
|
|
XM_011542840.3:c.2332A>T
|
XP_011541142.1:p.Asn778Tyr
|
|
XM_011542841.1:c.2332A>T
|
XP_011541143.1:p.Asn778Tyr
|
|
XM_011542842.1:c.2167A>T
|
XP_011541144.1:p.Asn723Tyr
|
|
XM_011542842.3:c.2167A>T
|
XP_011541144.1:p.Asn723Tyr
|
|
XM_011542843.1:c.2332A>T
|
XP_011541145.1:p.Asn778Tyr
|
|
XM_011542843.2:c.2332A>T
|
XP_011541145.1:p.Asn778Tyr
|
|
XM_011542844.1:c.1288A>T
|
XP_011541146.1:p.Asn430Tyr
|
|
XM_011542844.3:c.1288A>T
|
XP_011541146.1:p.Asn430Tyr
|
|
XM_011542845.1:c.1024A>T
|
XP_011541147.1:p.Asn342Tyr
|
|
XM_011542845.2:c.1024A>T
|
XP_011541147.1:p.Asn342Tyr
|
|
XM_011542846.1:c.2332A>T
|
XP_011541148.1:p.Asn778Tyr
|
|
XM_017017789.2:c.2332A>T
|
XP_016873278.1:p.Asn778Tyr
|
|
XM_017017790.2:c.2332A>T
|
XP_016873279.1:p.Asn778Tyr
|
|
XM_017017791.1:c.2332A>T
|
XP_016873280.1:p.Asn778Tyr
|
|
XM_017017792.2:c.2332A>T
|
XP_016873281.1:p.Asn778Tyr
|
|
XR_002957150.1:n.3065A>T
|
|
