ENST00000452508.7:c.5598T>C
|
ENSP00000388058.2:p.Val1866=
|
|
ENST00000713593.1:c.*5069T>C
|
ENSP00000518889.1:n.*5069T>C
|
|
ENST00000278616.9:c.5598T>C
|
ENSP00000278616.4:p.Val1866=
|
|
ENST00000683174.1:n.7082T>C
|
|
|
ENST00000683524.1:n.822T>C
|
|
|
ENST00000684152.1:n.1312T>C
|
|
|
ENST00000527805.6:c.*662T>C
|
ENSP00000435747.2:n.*662T>C
|
|
ENST00000675595.1:c.*662T>C
|
ENSP00000502563.1:n.*662T>C
|
|
ENST00000675843.1:c.5598T>C
MANE Select
|
ENSP00000501606.1:p.Val1866=
|
|
ENST00000278616.8:c.5598T>C
|
ENSP00000278616.4:p.Val1866=
|
|
ENST00000452508.6:c.5598T>C
|
ENSP00000388058.2:p.Val1866=
|
|
ENST00000524792.5:n.1813T>C
|
|
|
ENST00000529588.5:c.110T>C
|
|
|
ENST00000533690.5:n.1002T>C
|
|
|
NM_000051.3:c.5598T>C , LRG_135t1:c.5598T>C
|
NP_000042.3:p.Val1866=
|
|
XM_005271561.3:c.5598T>C
|
XP_005271618.2:p.Val1866=
|
|
XM_005271562.3:c.5598T>C
|
XP_005271619.2:p.Val1866=
|
|
XM_006718843.2:c.5598T>C
|
XP_006718906.1:p.Val1866=
|
|
XM_006718845.1:c.1554T>C
|
XP_006718908.1:p.Val518=
|
|
XM_011542840.1:c.5598T>C
|
XP_011541142.1:p.Val1866=
|
|
XM_011542841.1:c.5598T>C
|
XP_011541143.1:p.Val1866=
|
|
XM_011542842.1:c.5433T>C
|
XP_011541144.1:p.Val1811=
|
|
XM_011542843.1:c.5598T>C
|
XP_011541145.1:p.Val1866=
|
|
XM_011542844.1:c.4554T>C
|
XP_011541146.1:p.Val1518=
|
|
XM_011542845.1:c.4290T>C
|
XP_011541147.1:p.Val1430=
|
|
XM_011542847.1:c.669T>C
|
XP_011541149.1:p.Val223=
|
|
NM_001351834.1:c.5598T>C
|
NP_001338763.1:p.Val1866=
|
|
XM_005271562.5:c.5598T>C
|
XP_005271619.2:p.Val1866=
|
|
XM_006718843.4:c.5598T>C
|
XP_006718906.1:p.Val1866=
|
|
XM_006718845.2:c.1554T>C
|
XP_006718908.1:p.Val518=
|
|
XM_011542840.3:c.5598T>C
|
XP_011541142.1:p.Val1866=
|
|
XM_011542842.3:c.5433T>C
|
XP_011541144.1:p.Val1811=
|
|
XM_011542843.2:c.5598T>C
|
XP_011541145.1:p.Val1866=
|
|
XM_011542844.3:c.4554T>C
|
XP_011541146.1:p.Val1518=
|
|
XM_011542845.2:c.4290T>C
|
XP_011541147.1:p.Val1430=
|
|
XM_017017789.2:c.5598T>C
|
XP_016873278.1:p.Val1866=
|
|
XM_017017790.2:c.5598T>C
|
XP_016873279.1:p.Val1866=
|
|
XM_017017791.1:c.5598T>C
|
XP_016873280.1:p.Val1866=
|
|
XR_002957150.1:n.6198T>C
|
|
|
NM_001351834.2:c.5598T>C
|
NP_001338763.1:p.Val1866=
|
|
NM_000051.4:c.5598T>C
MANE Select
|
NP_000042.3:p.Val1866=
|
|