ENST00000405460.9:c.7067A>G
MANE Select
|
ENSP00000384582.2:p.Gln2356Arg
|
|
ENST00000639431.1:c.265+16511A>G
|
ENSP00000491057.1:n.265+16511A>G
|
|
ENST00000639473.1:n.2526A>G
|
|
|
ENST00000640012.1:c.874A>G
|
|
|
ENST00000640374.1:n.211A>G
|
|
|
ENST00000640403.1:c.4358A>G
|
ENSP00000492531.1:p.Gln1453Arg
|
|
ENST00000640779.1:c.1796A>G
|
|
|
ENST00000405460.6:c.7067A>G
|
ENSP00000384582.2:p.Gln2356Arg
|
|
NM_032119.3:c.7067A>G
|
NP_115495.3:p.Gln2356Arg
|
|
NR_003149.1:n.7080A>G
|
|
|
XM_011543675.1:c.7064A>G
|
XP_011541977.1:p.Gln2355Arg
|
|
XM_011543676.1:c.6986A>G
|
XP_011541978.1:p.Gln2329Arg
|
|
XM_011543677.1:c.4370A>G
|
XP_011541979.1:p.Gln1457Arg
|
|
XM_011543678.1:c.7067A>G
|
XP_011541980.1:p.Gln2356Arg
|
|
XM_011543679.1:c.7067A>G
|
XP_011541981.1:p.Gln2356Arg
|
|
NM_032119.4:c.7067A>G
MANE Select
|
NP_115495.3:p.Gln2356Arg
|
|
XM_017009963.2:c.7067A>G
|
XP_016865452.1:p.Gln2356Arg
|
|
XM_017009964.2:c.7064A>G
|
XP_016865453.1:p.Gln2355Arg
|
|
XM_017009965.1:c.7064A>G
|
XP_016865454.1:p.Gln2355Arg
|
|
XM_017009966.2:c.6986A>G
|
XP_016865455.1:p.Gln2329Arg
|
|
XM_017009967.1:c.6971A>G
|
XP_016865456.1:p.Gln2324Arg
|
|
XM_017009968.2:c.7067A>G
|
XP_016865457.1:p.Gln2356Arg
|
|
XM_017009969.2:c.7067A>G
|
XP_016865458.1:p.Gln2356Arg
|
|
XM_017009970.2:c.7067A>G
|
XP_016865459.1:p.Gln2356Arg
|
|
XM_017009971.2:c.7067A>G
|
XP_016865460.1:p.Gln2356Arg
|
|
XM_017009972.1:c.185A>G
|
XP_016865461.1:p.Gln62Arg
|
|
XM_017009973.1:c.185A>G
|
XP_016865462.1:p.Gln62Arg
|
|
XM_017009974.2:c.7067A>G
|
XP_016865463.1:p.Gln2356Arg
|
|
NR_003149.2:n.7083A>G
|
|
|