|
ENST00000553106.6:c.937G=
MANE Select
|
ENSP00000448059.1:p.Ala313=
|
|
|
ENST00000307000.7:c.922G=
|
ENSP00000303500.2:p.Ala308=
|
|
|
ENST00000549247.6:n.696G=
|
|
|
|
ENST00000551114.2:n.599G=
|
|
|
|
ENST00000553106.5:c.937G=
|
ENSP00000448059.1:p.Ala313=
|
|
|
ENST00000635477.1:c.74-2496G=
|
|
|
|
ENST00000635528.1:n.452G=
|
|
|
|
NM_000277.1:c.937G=
|
NP_000268.1:p.Ala313=
|
|
|
XM_011538422.1:c.913-2496G=
|
XP_011536724.1:n.913-2496G=
|
|
|
NM_000277.2:c.937G=
|
NP_000268.1:p.Ala313=
|
|
|
NM_001354304.1:c.937G=
|
NP_001341233.1:p.Ala313=
|
|
|
NM_000277.3:c.937G=
MANE Select
|
NP_000268.1:p.Ala313=
|
|
|
NM_001354304.2:c.937G=
|
NP_001341233.1:p.Ala313=
|
|
