ENST00000703986.1:c.7478A>G
|
ENSP00000515603.1:p.His2493Arg
|
|
ENST00000703987.1:c.7526A>G
|
ENSP00000515604.1:p.His2509Arg
|
|
ENST00000704649.1:c.3685-1855A>G
|
ENSP00000515974.1:n.3685-1855A>G
|
|
ENST00000704650.1:c.7463A>G
|
ENSP00000515975.1:p.His2488Arg
|
|
ENST00000704651.1:c.7310A>G
|
ENSP00000515976.1:p.His2437Arg
|
|
ENST00000704652.1:c.6562A>G
|
|
|
ENST00000704654.1:c.4342A>G
|
|
|
ENST00000704655.1:c.3606A>G
|
ENSP00000515980.1:n.3606A>G
|
|
ENST00000704656.1:c.2914A>G
|
ENSP00000515981.1:n.2914A>G
|
|
ENST00000324545.9:c.7511A>G
|
ENSP00000316357.6:p.His2504Arg
|
|
ENST00000378308.7:c.7463A>G
MANE Select
|
ENSP00000367558.2:p.His2488Arg
|
|
ENST00000324545.8:c.7511A>G
|
ENSP00000316357.6:p.His2504Arg
|
|
ENST00000378308.6:c.7463A>G
|
ENSP00000367558.2:p.His2488Arg
|
|
NM_001039590.2:c.7511A>G
|
NP_001034679.2:p.His2504Arg
|
|
NM_001039591.2:c.7463A>G
|
NP_001034680.2:p.His2488Arg
|
|
XM_005272675.3:c.7526A>G
|
XP_005272732.1:p.His2509Arg
|
|
XM_005272676.3:c.7478A>G
|
XP_005272733.1:p.His2493Arg
|
|
XM_005272675.4:c.7526A>G
|
XP_005272732.1:p.His2509Arg
|
|
XM_005272676.4:c.7478A>G
|
XP_005272733.1:p.His2493Arg
|
|
NM_001039591.3:c.7463A>G
MANE Select
|
NP_001034680.2:p.His2488Arg
|
|
NM_001039590.3:c.7511A>G
|
NP_001034679.2:p.His2504Arg
|
|