ENST00000029410.10:c.176G=
MANE Select
|
ENSP00000029410.5:p.Arg59=
|
|
ENST00000029410.9:c.176G=
|
ENSP00000029410.5:p.Arg59=
|
|
ENST00000502420.1:n.155G=
|
|
|
ENST00000505433.5:c.176G=
|
ENSP00000425591.1:p.Arg59=
|
|
ENST00000505468.1:c.-167G=
|
ENSP00000420886.1:n.-167G=
|
|
ENST00000510761.1:c.-167G=
|
ENSP00000423438.1:n.-167G=
|
|
NM_007255.2:c.176G=
|
NP_009186.1:p.Arg59=
|
|
XM_005265805.2:c.-167G=
|
XP_005265862.1:n.-167G=
|
|
XM_006714816.2:c.-324G=
|
XP_006714879.1:n.-324G=
|
|
XM_011534421.1:c.-167G=
|
XP_011532723.1:n.-167G=
|
|
XM_006714816.4:c.-324G=
|
XP_006714879.1:n.-324G=
|
|
XM_017008999.2:c.-167G=
|
XP_016864488.1:n.-167G=
|
|
NM_007255.3:c.176G=
MANE Select
|
NP_009186.1:p.Arg59=
|
|