ENST00000706645.1:n.1573G=
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|
|
ENST00000281243.10:c.526G=
MANE Select
|
ENSP00000281243.5:p.Ala176=
|
|
ENST00000281243.9:c.526G=
|
ENSP00000281243.5:p.Ala176=
|
|
ENST00000428702.6:c.433G=
|
ENSP00000390944.2:p.Ala145=
|
|
ENST00000501943.6:n.263G=
|
|
|
ENST00000505710.1:c.364-1506G=
|
|
|
ENST00000507439.5:c.437-1506G=
|
ENSP00000423227.1:n.437-1506G=
|
|
ENST00000508623.5:c.437-5015G=
|
ENSP00000426377.1:n.437-5015G=
|
|
ENST00000511609.1:n.258G=
|
|
|
ENST00000513615.5:c.437-1506G=
|
ENSP00000422759.1:n.437-1506G=
|
|
ENST00000514300.1:c.*368-1506G=
|
ENSP00000426039.1:n.*368-1506G=
|
|
NM_000320.2:c.526G=
|
NP_000311.2:p.Ala176=
|
|
NM_001306140.1:c.433G=
|
NP_001293069.1:p.Ala145=
|
|
XR_241677.1:n.600-1506G=
|
|
|
NR_156494.1:n.617-1506G=
|
|
|
NM_000320.3:c.526G=
MANE Select
|
NP_000311.2:p.Ala176=
|
|
NM_001306140.2:c.433G=
|
NP_001293069.1:p.Ala145=
|
|
NR_156494.2:n.473-1506G=
|
|
|