ENST00000400521.7:c.811C>G
MANE Select
|
ENSP00000383365.1:p.His271Asp
|
|
ENST00000334363.14:c.811C>G
|
ENSP00000334451.9:p.His271Asp
|
|
ENST00000400518.5:c.721C>G
|
ENSP00000383362.1:p.His241Asp
|
|
ENST00000400519.6:c.808C>G
|
ENSP00000383363.1:p.His270Asp
|
|
ENST00000400521.6:c.811C>G
|
ENSP00000383365.1:p.His271Asp
|
|
ENST00000400525.6:c.742C>G
|
ENSP00000383369.3:p.His248Asp
|
|
ENST00000474308.5:c.754C>G
|
ENSP00000485665.1:p.His252Asp
|
|
ENST00000475995.3:c.308C>G
|
|
|
ENST00000491939.6:c.715C>G
|
ENSP00000485543.1:p.His239Asp
|
|
ENST00000494454.5:n.885C>G
|
|
|
ENST00000542719.6:c.523C>G
|
ENSP00000485128.2:p.His175Asp
|
|
ENST00000634537.1:c.40C>G
|
ENSP00000489208.1:p.His14Asp
|
|
ENST00000635155.1:n.397C>G
|
|
|
NM_001282512.1:c.811C>G
|
NP_001269441.1:p.His271Asp
|
|
NM_006440.4:c.811C>G
|
NP_006431.2:p.His271Asp
|
|
NM_001282512.2:c.811C>G
|
NP_001269441.1:p.His271Asp
|
|
NM_001352300.1:c.808C>G
|
NP_001339229.1:p.His270Asp
|
|
NM_001352301.1:c.721C>G
|
NP_001339230.1:p.His241Asp
|
|
NM_001352302.1:c.523C>G
|
NP_001339231.1:p.His175Asp
|
|
NM_001352303.1:c.715C>G
|
NP_001339232.1:p.His239Asp
|
|
NR_147957.1:n.943C>G
|
|
|
NM_006440.5:c.811C>G
MANE Select
|
NP_006431.2:p.His271Asp
|
|
NM_001282512.3:c.811C>G
|
NP_001269441.1:p.His271Asp
|
|
NM_001352300.2:c.808C>G
|
NP_001339229.1:p.His270Asp
|
|
NR_147957.2:n.769C>G
|
|
|
NM_001352301.2:c.721C>G
|
NP_001339230.1:p.His241Asp
|
|
NM_001352302.2:c.523C>G
|
NP_001339231.1:p.His175Asp
|
|
NM_001352303.2:c.715C>G
|
NP_001339232.1:p.His239Asp
|
|