ENST00000496747.6:c.129A>C
|
ENSP00000417545.2:p.Gly43=
|
|
ENST00000703904.2:c.228A>C
|
ENSP00000515542.1:p.Gly76=
|
|
ENST00000703907.1:n.328A>C
|
|
|
ENST00000703908.1:c.228A>C
|
ENSP00000515545.1:p.Gly76=
|
|
ENST00000703909.1:c.228A>C
|
ENSP00000515546.1:p.Gly76=
|
|
ENST00000703910.1:c.228A>C
|
ENSP00000515547.1:p.Gly76=
|
|
ENST00000703911.1:c.228A>C
|
ENSP00000515548.1:p.Gly76=
|
|
ENST00000273398.8:c.228A>C
MANE Select
|
ENSP00000273398.3:p.Gly76=
|
|
ENST00000273398.7:c.228A>C
|
ENSP00000273398.3:p.Gly76=
|
|
ENST00000470455.5:c.*130A>C
|
ENSP00000420146.1:n.*130A>C
|
|
ENST00000475322.1:c.228A>C
|
ENSP00000419294.1:p.Gly76=
|
|
ENST00000496747.5:c.129A>C
|
ENSP00000417545.1:p.Gly43=
|
|
NM_001690.3:c.228A>C
|
NP_001681.2:p.Gly76=
|
|
NM_001690.4:c.228A>C
MANE Select
|
NP_001681.2:p.Gly76=
|
|