ENST00000706645.1:n.1592+302G=
|
|
|
ENST00000281243.10:c.545+302G=
MANE Select
|
ENSP00000281243.5:n.545+302G=
|
|
ENST00000281243.9:c.545+302G=
|
ENSP00000281243.5:n.545+302G=
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|
ENST00000428702.6:c.452+302G=
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ENSP00000390944.2:n.452+302G=
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|
ENST00000501943.6:n.282+302G=
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|
|
ENST00000505710.1:c.364-1185G=
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|
|
ENST00000507439.5:c.437-1185G=
|
ENSP00000423227.1:n.437-1185G=
|
|
ENST00000508623.5:c.437-4694G=
|
ENSP00000426377.1:n.437-4694G=
|
|
ENST00000511609.1:n.277+302G=
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|
|
ENST00000513615.5:c.437-1185G=
|
ENSP00000422759.1:n.437-1185G=
|
|
ENST00000514300.1:c.*368-1185G=
|
ENSP00000426039.1:n.*368-1185G=
|
|
NM_000320.2:c.545+302G=
|
NP_000311.2:n.545+302G=
|
|
NM_001306140.1:c.452+302G=
|
NP_001293069.1:n.452+302G=
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|
XR_241677.1:n.600-1185G=
|
|
|
NR_156494.1:n.617-1185G=
|
|
|
NM_000320.3:c.545+302G=
MANE Select
|
NP_000311.2:n.545+302G=
|
|
NM_001306140.2:c.452+302G=
|
NP_001293069.1:n.452+302G=
|
|
NR_156494.2:n.473-1185G=
|
|
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