|
ENST00000452508.7:c.5236G>C
|
ENSP00000388058.2:p.Gly1746Arg
|
|
|
ENST00000713593.1:c.*4707G>C
|
ENSP00000518889.1:n.*4707G>C
|
|
|
ENST00000278616.9:c.5236G>C
|
ENSP00000278616.4:p.Gly1746Arg
|
|
|
ENST00000683174.1:n.6720G>C
|
|
|
|
ENST00000683524.1:n.460G>C
|
|
|
|
ENST00000684152.1:n.950G>C
|
|
|
|
ENST00000527805.6:c.*300G>C
|
ENSP00000435747.2:n.*300G>C
|
|
|
ENST00000675595.1:c.*300G>C
|
ENSP00000502563.1:n.*300G>C
|
|
|
ENST00000675843.1:c.5236G>C
MANE Select
|
ENSP00000501606.1:p.Gly1746Arg
|
|
|
ENST00000278616.8:c.5236G>C
|
ENSP00000278616.4:p.Gly1746Arg
|
|
|
ENST00000452508.6:c.5236G>C
|
ENSP00000388058.2:p.Gly1746Arg
|
|
|
ENST00000524792.5:n.1451G>C
|
|
|
|
ENST00000533690.5:n.640G>C
|
|
|
|
ENST00000534625.1:n.465G>C
|
|
|
|
NM_000051.3:c.5236G>C , LRG_135t1:c.5236G>C
|
NP_000042.3:p.Gly1746Arg
|
|
|
XM_005271561.3:c.5236G>C
|
XP_005271618.2:p.Gly1746Arg
|
|
|
XM_005271562.3:c.5236G>C
|
XP_005271619.2:p.Gly1746Arg
|
|
|
XM_006718843.2:c.5236G>C
|
XP_006718906.1:p.Gly1746Arg
|
|
|
XM_006718845.1:c.1192G>C
|
XP_006718908.1:p.Gly398Arg
|
|
|
XM_011542840.1:c.5236G>C
|
XP_011541142.1:p.Gly1746Arg
|
|
|
XM_011542841.1:c.5236G>C
|
XP_011541143.1:p.Gly1746Arg
|
|
|
XM_011542842.1:c.5071G>C
|
XP_011541144.1:p.Gly1691Arg
|
|
|
XM_011542843.1:c.5236G>C
|
XP_011541145.1:p.Gly1746Arg
|
|
|
XM_011542844.1:c.4192G>C
|
XP_011541146.1:p.Gly1398Arg
|
|
|
XM_011542845.1:c.3928G>C
|
XP_011541147.1:p.Gly1310Arg
|
|
|
XM_011542846.1:c.5236G>C
|
XP_011541148.1:p.Gly1746Arg
|
|
|
XM_011542847.1:c.307G>C
|
XP_011541149.1:p.Gly103Arg
|
|
|
NM_001351834.1:c.5236G>C
|
NP_001338763.1:p.Gly1746Arg
|
|
|
XM_005271562.5:c.5236G>C
|
XP_005271619.2:p.Gly1746Arg
|
|
|
XM_006718843.4:c.5236G>C
|
XP_006718906.1:p.Gly1746Arg
|
|
|
XM_006718845.2:c.1192G>C
|
XP_006718908.1:p.Gly398Arg
|
|
|
XM_011542840.3:c.5236G>C
|
XP_011541142.1:p.Gly1746Arg
|
|
|
XM_011542842.3:c.5071G>C
|
XP_011541144.1:p.Gly1691Arg
|
|
|
XM_011542843.2:c.5236G>C
|
XP_011541145.1:p.Gly1746Arg
|
|
|
XM_011542844.3:c.4192G>C
|
XP_011541146.1:p.Gly1398Arg
|
|
|
XM_011542845.2:c.3928G>C
|
XP_011541147.1:p.Gly1310Arg
|
|
|
XM_017017789.2:c.5236G>C
|
XP_016873278.1:p.Gly1746Arg
|
|
|
XM_017017790.2:c.5236G>C
|
XP_016873279.1:p.Gly1746Arg
|
|
|
XM_017017791.1:c.5236G>C
|
XP_016873280.1:p.Gly1746Arg
|
|
|
XM_017017792.2:c.5236G>C
|
XP_016873281.1:p.Gly1746Arg
|
|
|
XR_002957150.1:n.5836G>C
|
|
|
|
NM_001351834.2:c.5236G>C
|
NP_001338763.1:p.Gly1746Arg
|
|
|
NM_000051.4:c.5236G>C
MANE Select
|
NP_000042.3:p.Gly1746Arg
|
|
