ENST00000405460.9:c.7099A>T
MANE Select
|
ENSP00000384582.2:p.Arg2367Ter
|
|
ENST00000639431.1:c.265+16543A>T
|
ENSP00000491057.1:n.265+16543A>T
|
|
ENST00000639473.1:n.2558A>T
|
|
|
ENST00000640012.1:c.906A>T
|
|
|
ENST00000640374.1:n.243A>T
|
|
|
ENST00000640403.1:c.4390A>T
|
ENSP00000492531.1:p.Arg1464Ter
|
|
ENST00000640779.1:c.1828A>T
|
|
|
ENST00000405460.6:c.7099A>T
|
ENSP00000384582.2:p.Arg2367Ter
|
|
NM_032119.3:c.7099A>T
|
NP_115495.3:p.Arg2367Ter
|
|
NR_003149.1:n.7112A>T
|
|
|
XM_011543675.1:c.7096A>T
|
XP_011541977.1:p.Arg2366Ter
|
|
XM_011543676.1:c.7018A>T
|
XP_011541978.1:p.Arg2340Ter
|
|
XM_011543677.1:c.4402A>T
|
XP_011541979.1:p.Arg1468Ter
|
|
XM_011543678.1:c.7099A>T
|
XP_011541980.1:p.Arg2367Ter
|
|
XM_011543679.1:c.7099A>T
|
XP_011541981.1:p.Arg2367Ter
|
|
NM_032119.4:c.7099A>T
MANE Select
|
NP_115495.3:p.Arg2367Ter
|
|
XM_017009963.2:c.7099A>T
|
XP_016865452.1:p.Arg2367Ter
|
|
XM_017009964.2:c.7096A>T
|
XP_016865453.1:p.Arg2366Ter
|
|
XM_017009965.1:c.7096A>T
|
XP_016865454.1:p.Arg2366Ter
|
|
XM_017009966.2:c.7018A>T
|
XP_016865455.1:p.Arg2340Ter
|
|
XM_017009967.1:c.7003A>T
|
XP_016865456.1:p.Arg2335Ter
|
|
XM_017009968.2:c.7099A>T
|
XP_016865457.1:p.Arg2367Ter
|
|
XM_017009969.2:c.7099A>T
|
XP_016865458.1:p.Arg2367Ter
|
|
XM_017009970.2:c.7099A>T
|
XP_016865459.1:p.Arg2367Ter
|
|
XM_017009971.2:c.7099A>T
|
XP_016865460.1:p.Arg2367Ter
|
|
XM_017009972.1:c.217A>T
|
XP_016865461.1:p.Arg73Ter
|
|
XM_017009973.1:c.217A>T
|
XP_016865462.1:p.Arg73Ter
|
|
XM_017009974.2:c.7099A>T
|
XP_016865463.1:p.Arg2367Ter
|
|
NR_003149.2:n.7115A>T
|
|
|