ENST00000382103.7:c.990A>T
MANE Select
|
ENSP00000371535.2:p.Gly330=
|
|
ENST00000680581.1:c.990A>T
|
ENSP00000506483.1:p.Gly330=
|
|
ENST00000680824.1:n.2206A>T
|
|
|
ENST00000681071.1:n.1282A>T
|
|
|
ENST00000681341.1:n.2131A>T
|
|
|
ENST00000681948.1:c.1245A>T
|
ENSP00000505991.1:p.Gly415=
|
|
ENST00000358971.7:c.*788A>T
|
ENSP00000351857.3:n.*788A>T
|
|
ENST00000382103.6:c.990A>T
|
ENSP00000371535.2:p.Gly330=
|
|
ENST00000503150.1:c.272A>T
|
|
|
ENST00000505513.1:n.290A>T
|
|
|
ENST00000514585.5:c.*691A>T
|
ENSP00000421880.1:n.*691A>T
|
|
NM_016955.3:c.990A>T
|
NP_058651.3:p.Gly330=
|
|
XM_005248168.2:c.753A>T
|
XP_005248225.1:p.Gly251=
|
|
XM_006713965.2:c.810A>T
|
XP_006714028.1:p.Gly270=
|
|
XM_011513846.1:c.987A>T
|
XP_011512148.1:p.Gly329=
|
|
XM_011513847.1:c.957A>T
|
XP_011512149.1:p.Gly319=
|
|
XM_011513848.1:c.810A>T
|
XP_011512150.1:p.Gly270=
|
|
XM_011513846.2:c.987A>T
|
XP_011512148.1:p.Gly329=
|
|
XM_011513847.2:c.957A>T
|
XP_011512149.1:p.Gly319=
|
|
XM_017008277.1:c.1245A>T
|
XP_016863766.1:p.Gly415=
|
|
XM_017008278.1:c.567A>T
|
XP_016863767.1:p.Gly189=
|
|
NM_016955.4:c.990A>T
MANE Select
|
NP_058651.3:p.Gly330=
|
|