|
ENST00000356839.10:c.542A>G
MANE Select
|
ENSP00000349297.5:p.His181Arg
|
|
|
ENST00000322910.9:c.*497A>G
|
ENSP00000325395.5:n.*497A>G
|
|
|
ENST00000350303.9:c.476A>G
|
ENSP00000344152.5:p.His159Arg
|
|
|
ENST00000356839.9:c.542A>G
|
ENSP00000349297.5:p.His181Arg
|
|
|
ENST00000543245.6:c.611A>G
|
ENSP00000438689.2:p.His204Arg
|
|
|
ENST00000577191.5:n.619A>G
|
|
|
|
ENST00000577433.5:n.750A>G
|
|
|
|
ENST00000577857.5:n.358A>G
|
|
|
|
ENST00000579286.5:n.723A>G
|
|
|
|
ENST00000579886.2:c.380A>G
|
ENSP00000463246.1:p.His127Arg
|
|
|
ENST00000580365.1:n.273A>G
|
|
|
|
ENST00000581378.5:c.260A>G
|
|
|
|
ENST00000581562.5:n.525-350A>G
|
|
|
|
ENST00000582166.1:n.523A>G
|
|
|
|
ENST00000583312.5:c.542A>G
|
ENSP00000467920.1:p.His181Arg
|
|
|
ENST00000583760.1:n.324A>G
|
|
|
|
NM_000018.3:c.542A>G
|
NP_000009.1:p.His181Arg
|
|
|
NM_001033859.2:c.476A>G
|
NP_001029031.1:p.His159Arg
|
|
|
NM_001270447.1:c.611A>G
|
NP_001257376.1:p.His204Arg
|
|
|
NM_001270448.1:c.314A>G
|
NP_001257377.1:p.His105Arg
|
|
|
XM_006721516.2:c.542A>G
|
XP_006721579.2:p.His181Arg
|
|
|
XM_011523829.1:c.542A>G
|
XP_011522131.1:p.His181Arg
|
|
|
XM_011523830.1:c.542A>G
|
XP_011522132.1:p.His181Arg
|
|
|
XR_934021.1:n.649A>G
|
|
|
|
XR_934022.1:n.649A>G
|
|
|
|
XR_934023.1:n.649A>G
|
|
|
|
XM_006721516.3:c.542A>G
|
XP_006721579.2:p.His181Arg
|
|
|
XM_011523829.2:c.542A>G
|
XP_011522131.1:p.His181Arg
|
|
|
XM_011523830.2:c.542A>G
|
XP_011522132.1:p.His181Arg
|
|
|
XM_024450741.1:c.542A>G
|
XP_024306509.1:p.His181Arg
|
|
|
XR_934021.2:n.601A>G
|
|
|
|
XR_934022.2:n.601A>G
|
|
|
|
XR_934023.2:n.601A>G
|
|
|
|
NM_000018.4:c.542A>G
MANE Select
|
NP_000009.1:p.His181Arg
|
|
|
NM_001033859.3:c.476A>G
|
NP_001029031.1:p.His159Arg
|
|
|
NM_001270447.2:c.611A>G
|
NP_001257376.1:p.His204Arg
|
|
|
NM_001270448.2:c.314A>G
|
NP_001257377.1:p.His105Arg
|
|
