ENST00000369552.9:c.19A>C
MANE Select
|
ENSP00000358565.4:p.Asn7His
|
|
ENST00000369552.8:c.19A>C
|
ENSP00000358565.4:p.Asn7His
|
|
ENST00000369556.7:c.19A>C
|
ENSP00000358569.3:p.Asn7His
|
|
ENST00000369557.9:c.19A>C
|
ENSP00000358570.5:p.Asn7His
|
|
ENST00000464978.5:n.94A>C
|
|
|
ENST00000506888.5:n.558A>C
|
|
|
ENST00000507897.5:c.*63A>C
|
ENSP00000426769.1:n.*63A>C
|
|
ENST00000513191.1:n.512A>C
|
|
|
ENST00000544441.4:c.19A>C
|
ENSP00000438603.2:p.Asn7His
|
|
ENST00000622775.3:c.-39A>C
|
ENSP00000479535.1:n.-39A>C
|
|
NM_001168398.1:c.19A>C
|
NP_001161870.1:p.Asn7His
|
|
NM_006416.4:c.19A>C
|
NP_006407.1:p.Asn7His
|
|
NM_006416.5:c.19A>C
MANE Select
|
NP_006407.1:p.Asn7His
|
|
NM_001168398.2:c.19A>C
|
NP_001161870.1:p.Asn7His
|
|