ENST00000261609.13:c.11882A>G
MANE Select
|
ENSP00000261609.8:p.His3961Arg
|
|
ENST00000650509.1:c.3593A>G
|
ENSP00000496936.1:p.His1198Arg
|
|
ENST00000261609.11:c.11882A>G
|
ENSP00000261609.7:p.His3961Arg
|
|
NM_004667.5:c.11882A>G
|
NP_004658.3:p.His3961Arg
|
|
XM_005268276.3:c.11768A>G
|
XP_005268333.1:p.His3923Arg
|
|
XM_005268277.3:c.11768A>G
|
XP_005268334.1:p.His3923Arg
|
|
XM_006720726.2:c.11867A>G
|
XP_006720789.1:p.His3956Arg
|
|
XM_006720727.2:c.11624A>G
|
XP_006720790.1:p.His3875Arg
|
|
XM_011522131.1:c.11399A>G
|
XP_011520433.1:p.His3800Arg
|
|
XM_011522132.1:c.9398A>G
|
XP_011520434.1:p.His3133Arg
|
|
XM_011522133.1:c.8627A>G
|
XP_011520435.1:p.His2876Arg
|
|
XM_011522134.1:c.5999A>G
|
XP_011520436.1:p.His2000Arg
|
|
XM_005268276.5:c.11768A>G
|
XP_005268333.1:p.His3923Arg
|
|
XM_006720726.3:c.11867A>G
|
XP_006720789.1:p.His3956Arg
|
|
XM_006720727.3:c.11624A>G
|
XP_006720790.1:p.His3875Arg
|
|
XM_017022695.1:c.11768A>G
|
XP_016878184.1:p.His3923Arg
|
|
XM_017022696.1:c.11768A>G
|
XP_016878185.1:p.His3923Arg
|
|
XM_017022697.1:c.5048A>G
|
XP_016878186.1:p.His1683Arg
|
|
XM_017022698.1:c.5048A>G
|
XP_016878187.1:p.His1683Arg
|
|
NM_004667.6:c.11882A>G
MANE Select
|
NP_004658.3:p.His3961Arg
|
|