NM_018026.4:c.399A>G
MANE Select
|
NP_060496.2:p.Glu133=
|
ENST00000320580.9:c.399A>G
MANE Select
|
ENSP00000316454.4:p.Glu133=
|
NM_018026.3:c.399A>G
|
NP_060496.2:p.Glu133=
|
ENST00000320580.8:c.399A>G
|
ENSP00000316454.4:p.Glu133=
|
ENST00000527224.1:n.523A>G
|
|
ENST00000527380.1:c.105A>G
|
ENSP00000432639.1:p.Glu35=
|
ENST00000533756.5:c.90A>G
|
ENSP00000437150.1:p.Glu30=
|
XM_011545162.1:c.78A>G
|
XP_011543464.1:p.Glu26=
|
XM_011545163.1:c.69A>G
|
XP_011543465.1:p.Glu23=
|
XM_011545164.1:c.60A>G
|
XP_011543466.1:p.Glu20=
|
XM_011545164.2:c.60A>G
|
XP_011543466.1:p.Glu20=
|
XR_001747924.1:n.610A>G
|
|