ENST00000261609.13:c.11764C>T
MANE Select
|
ENSP00000261609.8:p.His3922Tyr
|
|
ENST00000650509.1:c.3475C>T
|
ENSP00000496936.1:p.His1159Tyr
|
|
ENST00000261609.11:c.11764C>T
|
ENSP00000261609.7:p.His3922Tyr
|
|
ENST00000564519.1:n.279C>T
|
|
|
NM_004667.5:c.11764C>T
|
NP_004658.3:p.His3922Tyr
|
|
XM_005268276.3:c.11650C>T
|
XP_005268333.1:p.His3884Tyr
|
|
XM_005268277.3:c.11650C>T
|
XP_005268334.1:p.His3884Tyr
|
|
XM_006720726.2:c.11749C>T
|
XP_006720789.1:p.His3917Tyr
|
|
XM_006720727.2:c.11506C>T
|
XP_006720790.1:p.His3836Tyr
|
|
XM_011522131.1:c.11281C>T
|
XP_011520433.1:p.His3761Tyr
|
|
XM_011522132.1:c.9280C>T
|
XP_011520434.1:p.His3094Tyr
|
|
XM_011522133.1:c.8509C>T
|
XP_011520435.1:p.His2837Tyr
|
|
XM_011522134.1:c.5881C>T
|
XP_011520436.1:p.His1961Tyr
|
|
XM_005268276.5:c.11650C>T
|
XP_005268333.1:p.His3884Tyr
|
|
XM_006720726.3:c.11749C>T
|
XP_006720789.1:p.His3917Tyr
|
|
XM_006720727.3:c.11506C>T
|
XP_006720790.1:p.His3836Tyr
|
|
XM_017022695.1:c.11650C>T
|
XP_016878184.1:p.His3884Tyr
|
|
XM_017022696.1:c.11650C>T
|
XP_016878185.1:p.His3884Tyr
|
|
XM_017022697.1:c.4930C>T
|
XP_016878186.1:p.His1644Tyr
|
|
XM_017022698.1:c.4930C>T
|
XP_016878187.1:p.His1644Tyr
|
|
NM_004667.6:c.11764C>T
MANE Select
|
NP_004658.3:p.His3922Tyr
|
|