ENST00000541562.6:c.2173C>A
|
ENSP00000441000.2:p.His725Asn
|
|
ENST00000672801.1:c.2167C>A
|
ENSP00000500615.1:p.His723Asn
|
|
ENST00000676266.1:c.2173C>A
MANE Select
|
ENSP00000502585.1:p.His725Asn
|
|
ENST00000321897.9:c.2173C>A
|
ENSP00000316092.5:p.His725Asn
|
|
ENST00000469358.5:n.2161C>A
|
|
|
ENST00000476162.5:n.960C>A
|
|
|
ENST00000477052.1:n.259C>A
|
|
|
ENST00000477288.5:n.4786C>A
|
|
|
ENST00000541562.5:c.2263C>A
|
ENSP00000441000.1:p.His755Asn
|
|
ENST00000542001.5:c.2167C>A
|
ENSP00000438200.2:p.His723Asn
|
|
ENST00000625423.2:c.1753C>A
|
ENSP00000485818.1:p.His585Asn
|
|
NM_001167733.2:c.1753C>A
|
NP_001161205.1:p.His585Asn
|
|
NM_001167734.1:c.2263C>A
|
NP_001161206.1:p.His755Asn
|
|
NM_020442.5:c.2173C>A
|
NP_065175.4:p.His725Asn
|
|
NM_001167733.3:c.1753C>A
|
NP_001161205.1:p.His585Asn
|
|
NM_001167734.2:c.2263C>A
|
NP_001161206.1:p.His755Asn
|
|
NM_020442.6:c.2173C>A
MANE Select
|
NP_065175.4:p.His725Asn
|
|