ENST00000244020.5:c.768C>G
MANE Select
|
ENSP00000244020.3:p.Gly256=
|
|
ENST00000657241.1:c.654+198C>G
|
|
|
ENST00000662078.1:c.674+198C>G
|
ENSP00000499666.1:n.674+198C>G
|
|
ENST00000668808.1:c.768C>G
|
ENSP00000499517.1:p.Gly256=
|
|
ENST00000670741.1:c.674+198C>G
|
ENSP00000499492.1:n.674+198C>G
|
|
ENST00000671022.1:n.858C>G
|
|
|
ENST00000244020.4:c.768C>G
|
ENSP00000244020.3:p.Gly256=
|
|
ENST00000483871.6:c.*628C>G
|
ENSP00000433544.1:n.*628C>G
|
|
NM_006275.5:c.768C>G
|
NP_006266.2:p.Gly256=
|
|
NR_034009.1:n.1206C>G
|
|
|
XR_936608.1:n.1527C>G
|
|
|
XR_936608.2:n.1527C>G
|
|
|
NM_006275.6:c.768C>G
MANE Select
|
NP_006266.2:p.Gly256=
|
|
NR_034009.2:n.1174C>G
|
|
|