ENST00000263038.9:c.788T>A
MANE Select
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ENSP00000263038.4:p.Ile263Asn
|
|
ENST00000263038.8:c.788T>A
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ENSP00000263038.4:p.Ile263Asn
|
|
ENST00000396913.6:c.488T>A
|
ENSP00000380121.2:p.Ile163Asn
|
|
ENST00000396920.7:c.737T>A
|
ENSP00000380126.3:p.Ile246Asn
|
|
ENST00000453759.6:c.488T>A
|
ENSP00000412525.2:p.Ile163Asn
|
|
NM_001037537.1:c.488T>A
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NP_001032626.1:p.Ile163Asn
|
|
NM_006214.3:c.788T>A
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NP_006205.1:p.Ile263Asn
|
|
XM_005252469.2:c.569T>A
|
XP_005252526.1:p.Ile190Asn
|
|
NM_001323080.1:c.488T>A
|
NP_001310009.1:p.Ile163Asn
|
|
NM_001323082.1:c.794T>A
|
NP_001310011.1:p.Ile265Asn
|
|
NM_001323083.1:c.524T>A
|
NP_001310012.1:p.Ile175Asn
|
|
NM_001323084.1:c.494T>A
|
NP_001310013.1:p.Ile165Asn
|
|
NM_006214.4:c.788T>A
MANE Select
|
NP_006205.1:p.Ile263Asn
|
|
NM_001037537.2:c.488T>A
|
NP_001032626.1:p.Ile163Asn
|
|
NM_001323080.2:c.488T>A
|
NP_001310009.1:p.Ile163Asn
|
|
NM_001323082.2:c.794T>A
|
NP_001310011.1:p.Ile265Asn
|
|
NM_001323083.2:c.524T>A
|
NP_001310012.1:p.Ile175Asn
|
|
NM_001323084.2:c.494T>A
|
NP_001310013.1:p.Ile165Asn
|
|