ENST00000302068.9:c.1063C>A
MANE Select
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ENSP00000306099.4:p.His355Asn
|
|
ENST00000302068.8:c.1063C>A
|
ENSP00000306099.4:p.His355Asn
|
|
ENST00000502545.5:n.939+311C>A
|
|
|
ENST00000509493.1:c.406C>A
|
ENSP00000426757.1:p.His136Asn
|
|
NM_001184741.1:c.886C>A
|
NP_001171670.1:p.His296Asn
|
|
NM_005141.4:c.1063C>A , LRG_558t1:c.1063C>A
|
NP_005132.2:p.His355Asn
|
|
NM_001382759.1:c.931C>A
|
NP_001369688.1:p.His311Asn
|
|
NM_001382760.1:c.1063C>A
|
NP_001369689.1:p.His355Asn
|
|
NM_001382761.1:c.1063C>A
|
NP_001369690.1:p.His355Asn
|
|
NM_001382762.1:c.763C>A
|
NP_001369691.1:p.His255Asn
|
|
NM_001382763.1:c.1054C>A
|
NP_001369692.1:p.His352Asn
|
|
NM_001382764.1:c.1063C>A
|
NP_001369693.1:p.His355Asn
|
|
NM_001382765.1:c.1063C>A
|
NP_001369694.1:p.His355Asn
|
|
NM_005141.5:c.1063C>A
MANE Select
|
NP_005132.2:p.His355Asn
|
|