ENST00000700029.2:c.-787G=
|
ENSP00000514759.2:n.-787G=
|
|
ENST00000710265.1:c.-787G=
|
ENSP00000518161.1:n.-787G=
|
|
ENST00000706954.1:c.-16-771G=
|
ENSP00000516674.1:n.-16-771G=
|
|
ENST00000706955.1:c.-787G=
|
ENSP00000516675.1:n.-787G=
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|
ENST00000688158.1:c.-787G=
|
ENSP00000509254.1:n.-787G=
|
|
ENST00000688308.1:c.-17+570G=
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ENSP00000508752.1:n.-17+570G=
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ENST00000693560.1:c.-267G=
|
ENSP00000509861.1:n.-267G=
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|
ENST00000371953.8:c.-787G=
MANE Select
|
ENSP00000361021.3:n.-787G=
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ENST00000371953.7:c.-787G=
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ENSP00000361021.3:n.-787G=
|
|
ENST00000610634.1:c.-889G=
|
ENSP00000477517.1:n.-889G=
|
|
NM_000314.5:c.-786G=
|
NP_000305.3:n.-786G=
|
|
NM_000314.6:c.-786G=
|
NP_000305.3:n.-786G=
|
|
NM_001304717.2:c.-267G=
|
NP_001291646.2:n.-267G=
|
|
NM_001304718.1:c.-1491G=
|
NP_001291647.1:n.-1491G=
|
|
NM_000314.7:c.-786G=
|
NP_000305.3:n.-786G=
|
|
NM_001304717.5:c.-267G=
|
NP_001291646.4:n.-267G=
|
|
NM_001304718.2:c.-1491G=
|
NP_001291647.1:n.-1491G=
|
|
NM_000314.8:c.-787G=
MANE Select
|
NP_000305.3:n.-787G=
|
|