|
ENST00000375687.10:c.439A>G
MANE Select
|
ENSP00000364839.4:p.Asn147Asp
|
|
|
ENST00000470145.3:n.458A>G
|
|
|
|
ENST00000643168.1:c.355A>G
|
ENSP00000495003.1:p.Asn119Asp
|
|
|
ENST00000644587.1:c.*278A>G
|
ENSP00000494813.1:n.*278A>G
|
|
|
ENST00000644615.1:n.143A>G
|
|
|
|
ENST00000645514.1:n.263A>G
|
|
|
|
ENST00000646985.1:c.409A>G
|
ENSP00000495053.1:p.Asn137Asp
|
|
|
ENST00000651418.1:c.439A>G
|
ENSP00000499150.1:p.Asn147Asp
|
|
|
ENST00000306058.9:c.424A>G
|
ENSP00000305119.5:p.Asn142Asp
|
|
|
ENST00000375687.8:c.439A>G
|
ENSP00000364839.4:p.Asn147Asp
|
|
|
ENST00000470145.2:n.458A>G
|
|
|
|
ENST00000613218.4:c.439A>G
|
ENSP00000480487.1:p.Asn147Asp
|
|
|
ENST00000620121.4:c.439A>G
|
ENSP00000481978.1:p.Asn147Asp
|
|
|
NM_015338.5:c.439A>G , LRG_630t1:c.439A>G
|
NP_056153.2:p.Asn147Asp
|
|
|
XM_006723727.2:c.436A>G
|
XP_006723790.1:p.Asn146Asp
|
|
|
XM_006723728.2:c.409A>G
|
XP_006723791.1:p.Asn137Asp
|
|
|
XM_006723730.2:c.355A>G
|
XP_006723793.1:p.Asn119Asp
|
|
|
XM_006723732.2:c.409A>G
|
XP_006723795.1:p.Asn137Asp
|
|
|
XM_011528647.1:c.703A>G
|
XP_011526949.1:p.Asn235Asp
|
|
|
XM_011528648.1:c.700A>G
|
XP_011526950.1:p.Asn234Asp
|
|
|
XM_011528649.1:c.619A>G
|
XP_011526951.1:p.Asn207Asp
|
|
|
XM_011528650.1:c.703A>G
|
XP_011526952.1:p.Asn235Asp
|
|
|
XM_011528651.1:c.418A>G
|
XP_011526953.1:p.Asn140Asp
|
|
|
XM_011528652.1:c.355A>G
|
XP_011526954.1:p.Asn119Asp
|
|
|
NM_001363734.1:c.409A>G
|
NP_001350663.1:p.Asn137Asp
|
|
|
XM_006723727.3:c.436A>G
|
XP_006723790.1:p.Asn146Asp
|
|
|
XM_006723728.3:c.409A>G
|
XP_006723791.1:p.Asn137Asp
|
|
|
XM_006723730.4:c.355A>G
|
XP_006723793.1:p.Asn119Asp
|
|
|
XM_011528648.3:c.700A>G
|
XP_011526950.1:p.Asn234Asp
|
|
|
XM_011528652.2:c.355A>G
|
XP_011526954.1:p.Asn119Asp
|
|
|
XM_017027704.1:c.355A>G
|
XP_016883193.1:p.Asn119Asp
|
|
|
XM_017027705.1:c.355A>G
|
XP_016883194.1:p.Asn119Asp
|
|
|
XM_017027706.1:c.439A>G
|
XP_016883195.1:p.Asn147Asp
|
|
|
NM_015338.6:c.439A>G
MANE Select
|
NP_056153.2:p.Asn147Asp
|
|
