ENST00000405460.9:c.10806A>G
MANE Select
|
ENSP00000384582.2:p.Glu3602=
|
|
ENST00000639431.1:c.265+69418A>G
|
ENSP00000491057.1:n.265+69418A>G
|
|
ENST00000640374.1:n.3950A>G
|
|
|
ENST00000640464.1:n.1225A>G
|
|
|
ENST00000405460.6:c.10806A>G
|
ENSP00000384582.2:p.Glu3602=
|
|
ENST00000509621.1:c.3503A>G
|
|
|
NM_032119.3:c.10806A>G
|
NP_115495.3:p.Glu3602=
|
|
NR_003149.1:n.10819A>G
|
|
|
XM_011543675.1:c.10803A>G
|
XP_011541977.1:p.Glu3601=
|
|
XM_011543676.1:c.10725A>G
|
XP_011541978.1:p.Glu3575=
|
|
XM_011543677.1:c.8109A>G
|
XP_011541979.1:p.Glu2703=
|
|
XM_011543678.1:c.10806A>G
|
XP_011541980.1:p.Glu3602=
|
|
XM_011543679.1:c.*28A>G
|
XP_011541981.1:n.*28A>G
|
|
NM_032119.4:c.10806A>G
MANE Select
|
NP_115495.3:p.Glu3602=
|
|
XM_017009963.2:c.10827A>G
|
XP_016865452.1:p.Glu3609=
|
|
XM_017009964.2:c.10824A>G
|
XP_016865453.1:p.Glu3608=
|
|
XM_017009965.1:c.10824A>G
|
XP_016865454.1:p.Glu3608=
|
|
XM_017009966.2:c.10746A>G
|
XP_016865455.1:p.Glu3582=
|
|
XM_017009967.1:c.10731A>G
|
XP_016865456.1:p.Glu3577=
|
|
XM_017009968.2:c.10827A>G
|
XP_016865457.1:p.Glu3609=
|
|
XM_017009969.2:c.10827A>G
|
XP_016865458.1:p.Glu3609=
|
|
XM_017009970.2:c.10827A>G
|
XP_016865459.1:p.Glu3609=
|
|
XM_017009971.2:c.10827A>G
|
XP_016865460.1:p.Glu3609=
|
|
XM_017009972.1:c.3945A>G
|
XP_016865461.1:p.Glu1315=
|
|
XM_017009973.1:c.3924A>G
|
XP_016865462.1:p.Glu1308=
|
|
XM_017009974.2:c.*28A>G
|
XP_016865463.1:n.*28A>G
|
|
NR_003149.2:n.10822A>G
|
|
|