ENST00000405460.9:c.10803A>G
MANE Select
|
ENSP00000384582.2:p.Arg3601=
|
|
ENST00000639431.1:c.265+69415A>G
|
ENSP00000491057.1:n.265+69415A>G
|
|
ENST00000640374.1:n.3947A>G
|
|
|
ENST00000640464.1:n.1222A>G
|
|
|
ENST00000405460.6:c.10803A>G
|
ENSP00000384582.2:p.Arg3601=
|
|
ENST00000509621.1:c.3500A>G
|
|
|
NM_032119.3:c.10803A>G
|
NP_115495.3:p.Arg3601=
|
|
NR_003149.1:n.10816A>G
|
|
|
XM_011543675.1:c.10800A>G
|
XP_011541977.1:p.Arg3600=
|
|
XM_011543676.1:c.10722A>G
|
XP_011541978.1:p.Arg3574=
|
|
XM_011543677.1:c.8106A>G
|
XP_011541979.1:p.Arg2702=
|
|
XM_011543678.1:c.10803A>G
|
XP_011541980.1:p.Arg3601=
|
|
XM_011543679.1:c.*25A>G
|
XP_011541981.1:n.*25A>G
|
|
NM_032119.4:c.10803A>G
MANE Select
|
NP_115495.3:p.Arg3601=
|
|
XM_017009963.2:c.10824A>G
|
XP_016865452.1:p.Arg3608=
|
|
XM_017009964.2:c.10821A>G
|
XP_016865453.1:p.Arg3607=
|
|
XM_017009965.1:c.10821A>G
|
XP_016865454.1:p.Arg3607=
|
|
XM_017009966.2:c.10743A>G
|
XP_016865455.1:p.Arg3581=
|
|
XM_017009967.1:c.10728A>G
|
XP_016865456.1:p.Arg3576=
|
|
XM_017009968.2:c.10824A>G
|
XP_016865457.1:p.Arg3608=
|
|
XM_017009969.2:c.10824A>G
|
XP_016865458.1:p.Arg3608=
|
|
XM_017009970.2:c.10824A>G
|
XP_016865459.1:p.Arg3608=
|
|
XM_017009971.2:c.10824A>G
|
XP_016865460.1:p.Arg3608=
|
|
XM_017009972.1:c.3942A>G
|
XP_016865461.1:p.Arg1314=
|
|
XM_017009973.1:c.3921A>G
|
XP_016865462.1:p.Arg1307=
|
|
XM_017009974.2:c.*25A>G
|
XP_016865463.1:n.*25A>G
|
|
NR_003149.2:n.10819A>G
|
|
|