ENST00000283871.10:c.874C>G
MANE Select
|
ENSP00000283871.5:p.His292Asp
|
|
ENST00000283871.9:c.874C>G
|
ENSP00000283871.5:p.His292Asp
|
|
ENST00000470321.1:n.214C>G
|
|
|
ENST00000475447.2:c.302C>G
|
|
|
ENST00000492108.5:c.280C>G
|
ENSP00000419838.1:p.His94Asp
|
|
ENST00000494453.1:c.294C>G
|
|
|
NM_000187.3:c.874C>G
|
NP_000178.2:p.His292Asp
|
|
XM_005247412.1:c.649C>G
|
XP_005247469.1:p.His217Asp
|
|
XM_005247413.1:c.874C>G
|
XP_005247470.1:p.His292Asp
|
|
XM_011512746.1:c.874C>G
|
XP_011511048.1:p.His292Asp
|
|
XM_005247412.2:c.649C>G
|
XP_005247469.1:p.His217Asp
|
|
XM_005247413.2:c.874C>G
|
XP_005247470.1:p.His292Asp
|
|
XM_011512746.2:c.874C>G
|
XP_011511048.1:p.His292Asp
|
|
XM_017006277.2:c.451C>G
|
XP_016861766.1:p.His151Asp
|
|
NM_000187.4:c.874C>G
MANE Select
|
NP_000178.2:p.His292Asp
|
|