ENST00000261609.13:c.11757T>A
MANE Select
|
ENSP00000261609.8:p.His3919Gln
|
|
ENST00000650509.1:c.3468T>A
|
ENSP00000496936.1:p.His1156Gln
|
|
ENST00000261609.11:c.11757T>A
|
ENSP00000261609.7:p.His3919Gln
|
|
ENST00000564519.1:n.272T>A
|
|
|
NM_004667.5:c.11757T>A
|
NP_004658.3:p.His3919Gln
|
|
XM_005268276.3:c.11643T>A
|
XP_005268333.1:p.His3881Gln
|
|
XM_005268277.3:c.11643T>A
|
XP_005268334.1:p.His3881Gln
|
|
XM_006720726.2:c.11742T>A
|
XP_006720789.1:p.His3914Gln
|
|
XM_006720727.2:c.11499T>A
|
XP_006720790.1:p.His3833Gln
|
|
XM_011522131.1:c.11274T>A
|
XP_011520433.1:p.His3758Gln
|
|
XM_011522132.1:c.9273T>A
|
XP_011520434.1:p.His3091Gln
|
|
XM_011522133.1:c.8502T>A
|
XP_011520435.1:p.His2834Gln
|
|
XM_011522134.1:c.5874T>A
|
XP_011520436.1:p.His1958Gln
|
|
XM_005268276.5:c.11643T>A
|
XP_005268333.1:p.His3881Gln
|
|
XM_006720726.3:c.11742T>A
|
XP_006720789.1:p.His3914Gln
|
|
XM_006720727.3:c.11499T>A
|
XP_006720790.1:p.His3833Gln
|
|
XM_017022695.1:c.11643T>A
|
XP_016878184.1:p.His3881Gln
|
|
XM_017022696.1:c.11643T>A
|
XP_016878185.1:p.His3881Gln
|
|
XM_017022697.1:c.4923T>A
|
XP_016878186.1:p.His1641Gln
|
|
XM_017022698.1:c.4923T>A
|
XP_016878187.1:p.His1641Gln
|
|
NM_004667.6:c.11757T>A
MANE Select
|
NP_004658.3:p.His3919Gln
|
|