ENST00000400521.7:c.799C>A
MANE Select
|
ENSP00000383365.1:p.His267Asn
|
|
ENST00000334363.14:c.799C>A
|
ENSP00000334451.9:p.His267Asn
|
|
ENST00000400518.5:c.709C>A
|
ENSP00000383362.1:p.His237Asn
|
|
ENST00000400519.6:c.796C>A
|
ENSP00000383363.1:p.His266Asn
|
|
ENST00000400521.6:c.799C>A
|
ENSP00000383365.1:p.His267Asn
|
|
ENST00000400525.6:c.730C>A
|
ENSP00000383369.3:p.His244Asn
|
|
ENST00000474308.5:c.742C>A
|
ENSP00000485665.1:p.His248Asn
|
|
ENST00000475995.3:c.296C>A
|
|
|
ENST00000491939.6:c.703C>A
|
ENSP00000485543.1:p.His235Asn
|
|
ENST00000494454.5:n.873C>A
|
|
|
ENST00000542719.6:c.511C>A
|
ENSP00000485128.2:p.His171Asn
|
|
ENST00000634537.1:c.28C>A
|
ENSP00000489208.1:p.His10Asn
|
|
ENST00000635155.1:n.385C>A
|
|
|
NM_001282512.1:c.799C>A
|
NP_001269441.1:p.His267Asn
|
|
NM_006440.4:c.799C>A
|
NP_006431.2:p.His267Asn
|
|
NM_001282512.2:c.799C>A
|
NP_001269441.1:p.His267Asn
|
|
NM_001352300.1:c.796C>A
|
NP_001339229.1:p.His266Asn
|
|
NM_001352301.1:c.709C>A
|
NP_001339230.1:p.His237Asn
|
|
NM_001352302.1:c.511C>A
|
NP_001339231.1:p.His171Asn
|
|
NM_001352303.1:c.703C>A
|
NP_001339232.1:p.His235Asn
|
|
NR_147957.1:n.931C>A
|
|
|
NM_006440.5:c.799C>A
MANE Select
|
NP_006431.2:p.His267Asn
|
|
NM_001282512.3:c.799C>A
|
NP_001269441.1:p.His267Asn
|
|
NM_001352300.2:c.796C>A
|
NP_001339229.1:p.His266Asn
|
|
NR_147957.2:n.757C>A
|
|
|
NM_001352301.2:c.709C>A
|
NP_001339230.1:p.His237Asn
|
|
NM_001352302.2:c.511C>A
|
NP_001339231.1:p.His171Asn
|
|
NM_001352303.2:c.703C>A
|
NP_001339232.1:p.His235Asn
|
|