ENST00000265517.10:c.376C>A
MANE Select
|
ENSP00000265517.5:p.His126Asn
|
|
ENST00000457717.6:c.376C>A
|
ENSP00000400821.1:p.His126Asn
|
|
ENST00000511045.6:c.127C>A
|
ENSP00000427679.2:p.His43Asn
|
|
ENST00000265517.9:c.376C>A
|
ENSP00000265517.5:p.His126Asn
|
|
ENST00000422897.6:c.376C>A
|
ENSP00000407350.2:p.His126Asn
|
|
ENST00000457717.5:c.376C>A
|
ENSP00000400821.1:p.His126Asn
|
|
ENST00000506883.5:c.406C>A
|
ENSP00000426755.1:p.His136Asn
|
|
ENST00000511045.5:c.457C>A
|
ENSP00000427679.1:p.His153Asn
|
|
ENST00000619629.1:c.376C>A
|
ENSP00000482850.1:p.His126Asn
|
|
NM_000253.3:c.376C>A
|
NP_000244.2:p.His126Asn
|
|
NM_001300785.1:c.457C>A
|
NP_001287714.1:p.His153Asn
|
|
NM_000253.4:c.376C>A
|
NP_000244.2:p.His126Asn
|
|
NM_001300785.2:c.127C>A
|
NP_001287714.2:p.His43Asn
|
|
NM_001386140.1:c.376C>A
MANE Select
|
NP_001373069.1:p.His126Asn
|
|