ENST00000682617.1:c.2767G=
|
ENSP00000507912.1:p.Ala923=
|
|
ENST00000683962.1:c.*2323G=
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ENSP00000506854.1:n.*2323G=
|
|
ENST00000311895.8:c.2629G=
MANE Select
|
ENSP00000310520.7:p.Ala877=
|
|
ENST00000311895.7:c.2629G=
|
ENSP00000310520.7:p.Ala877=
|
|
ENST00000389138.7:n.1906G=
|
|
|
NM_005236.2:c.2629G= , LRG_463t1:c.2629G=
|
NP_005227.1:p.Ala877=
|
|
XM_011522424.1:c.2767G=
|
XP_011520726.1:p.Ala923=
|
|
XM_011522425.1:c.2086G=
|
XP_011520727.1:p.Ala696=
|
|
XM_011522426.1:c.1840G=
|
XP_011520728.1:p.Ala614=
|
|
XM_011522427.1:c.1279G=
|
XP_011520729.1:p.Ala427=
|
|
XR_932805.1:n.2788G=
|
|
|
XM_011522424.3:c.2767G=
|
XP_011520726.1:p.Ala923=
|
|
XM_017023043.2:c.1840G=
|
XP_016878532.1:p.Ala614=
|
|
NM_005236.3:c.2629G=
MANE Select
|
NP_005227.1:p.Ala877=
|
|