ENST00000375687.10:c.367A>C
MANE Select
|
ENSP00000364839.4:p.Asn123His
|
|
ENST00000470145.3:n.310A>C
|
|
|
ENST00000643168.1:c.283A>C
|
ENSP00000495003.1:p.Asn95His
|
|
ENST00000644060.1:n.1171A>C
|
|
|
ENST00000644587.1:c.*206A>C
|
ENSP00000494813.1:n.*206A>C
|
|
ENST00000644615.1:n.71A>C
|
|
|
ENST00000645514.1:n.115A>C
|
|
|
ENST00000646985.1:c.337A>C
|
ENSP00000495053.1:p.Asn113His
|
|
ENST00000651418.1:c.367A>C
|
ENSP00000499150.1:p.Asn123His
|
|
ENST00000306058.9:c.352A>C
|
ENSP00000305119.5:p.Asn118His
|
|
ENST00000375687.8:c.367A>C
|
ENSP00000364839.4:p.Asn123His
|
|
ENST00000470145.2:n.310A>C
|
|
|
ENST00000613218.4:c.367A>C
|
ENSP00000480487.1:p.Asn123His
|
|
ENST00000620121.4:c.367A>C
|
ENSP00000481978.1:p.Asn123His
|
|
NM_015338.5:c.367A>C , LRG_630t1:c.367A>C
|
NP_056153.2:p.Asn123His
|
|
XM_006723727.2:c.364A>C
|
XP_006723790.1:p.Asn122His
|
|
XM_006723728.2:c.337A>C
|
XP_006723791.1:p.Asn113His
|
|
XM_006723730.2:c.283A>C
|
XP_006723793.1:p.Asn95His
|
|
XM_006723732.2:c.337A>C
|
XP_006723795.1:p.Asn113His
|
|
XM_011528647.1:c.631A>C
|
XP_011526949.1:p.Asn211His
|
|
XM_011528648.1:c.628A>C
|
XP_011526950.1:p.Asn210His
|
|
XM_011528649.1:c.547A>C
|
XP_011526951.1:p.Asn183His
|
|
XM_011528650.1:c.631A>C
|
XP_011526952.1:p.Asn211His
|
|
XM_011528651.1:c.346A>C
|
XP_011526953.1:p.Asn116His
|
|
XM_011528652.1:c.283A>C
|
XP_011526954.1:p.Asn95His
|
|
NM_001363734.1:c.337A>C
|
NP_001350663.1:p.Asn113His
|
|
XM_006723727.3:c.364A>C
|
XP_006723790.1:p.Asn122His
|
|
XM_006723728.3:c.337A>C
|
XP_006723791.1:p.Asn113His
|
|
XM_006723730.4:c.283A>C
|
XP_006723793.1:p.Asn95His
|
|
XM_011528648.3:c.628A>C
|
XP_011526950.1:p.Asn210His
|
|
XM_011528652.2:c.283A>C
|
XP_011526954.1:p.Asn95His
|
|
XM_017027704.1:c.283A>C
|
XP_016883193.1:p.Asn95His
|
|
XM_017027705.1:c.283A>C
|
XP_016883194.1:p.Asn95His
|
|
XM_017027706.1:c.367A>C
|
XP_016883195.1:p.Asn123His
|
|
NM_015338.6:c.367A>C
MANE Select
|
NP_056153.2:p.Asn123His
|
|