ENST00000315491.12:c.1327G=
MANE Select
|
ENSP00000320295.7:p.Glu443=
|
|
ENST00000680788.1:n.4748G=
|
|
|
ENST00000315491.11:c.1327G=
|
ENSP00000320295.7:p.Glu443=
|
|
ENST00000554444.5:c.1111G=
|
ENSP00000451617.1:p.Glu371=
|
|
ENST00000555576.5:c.277+2200G=
|
ENSP00000452554.1:n.277+2200G=
|
|
ENST00000555609.5:c.*1412G=
|
ENSP00000451276.1:n.*1412G=
|
|
ENST00000556922.1:c.2368G=
|
ENSP00000451560.1:p.Glu790=
|
|
NM_001197181.1:c.1111G=
|
NP_001184110.1:p.Glu371=
|
|
NM_006086.3:c.1327G=
|
NP_006077.2:p.Glu443=
|
|
NM_006086.4:c.1327G=
MANE Select
|
NP_006077.2:p.Glu443=
|
|
NM_001197181.2:c.1111G=
|
NP_001184110.1:p.Glu371=
|
|