ENST00000261609.13:c.11815A>T
MANE Select
|
ENSP00000261609.8:p.Arg3939Trp
|
|
ENST00000650509.1:c.3526A>T
|
ENSP00000496936.1:p.Arg1176Trp
|
|
ENST00000261609.11:c.11815A>T
|
ENSP00000261609.7:p.Arg3939Trp
|
|
NM_004667.5:c.11815A>T
|
NP_004658.3:p.Arg3939Trp
|
|
XM_005268276.3:c.11701A>T
|
XP_005268333.1:p.Arg3901Trp
|
|
XM_005268277.3:c.11701A>T
|
XP_005268334.1:p.Arg3901Trp
|
|
XM_006720726.2:c.11800A>T
|
XP_006720789.1:p.Arg3934Trp
|
|
XM_006720727.2:c.11557A>T
|
XP_006720790.1:p.Arg3853Trp
|
|
XM_011522131.1:c.11332A>T
|
XP_011520433.1:p.Arg3778Trp
|
|
XM_011522132.1:c.9331A>T
|
XP_011520434.1:p.Arg3111Trp
|
|
XM_011522133.1:c.8560A>T
|
XP_011520435.1:p.Arg2854Trp
|
|
XM_011522134.1:c.5932A>T
|
XP_011520436.1:p.Arg1978Trp
|
|
XM_005268276.5:c.11701A>T
|
XP_005268333.1:p.Arg3901Trp
|
|
XM_006720726.3:c.11800A>T
|
XP_006720789.1:p.Arg3934Trp
|
|
XM_006720727.3:c.11557A>T
|
XP_006720790.1:p.Arg3853Trp
|
|
XM_017022695.1:c.11701A>T
|
XP_016878184.1:p.Arg3901Trp
|
|
XM_017022696.1:c.11701A>T
|
XP_016878185.1:p.Arg3901Trp
|
|
XM_017022697.1:c.4981A>T
|
XP_016878186.1:p.Arg1661Trp
|
|
XM_017022698.1:c.4981A>T
|
XP_016878187.1:p.Arg1661Trp
|
|
NM_004667.6:c.11815A>T
MANE Select
|
NP_004658.3:p.Arg3939Trp
|
|