ENST00000261609.13:c.11884A>C
MANE Select
|
ENSP00000261609.8:p.Arg3962=
|
|
ENST00000650509.1:c.3595A>C
|
ENSP00000496936.1:p.Arg1199=
|
|
ENST00000261609.11:c.11884A>C
|
ENSP00000261609.7:p.Arg3962=
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|
NM_004667.5:c.11884A>C
|
NP_004658.3:p.Arg3962=
|
|
XM_005268276.3:c.11770A>C
|
XP_005268333.1:p.Arg3924=
|
|
XM_005268277.3:c.11770A>C
|
XP_005268334.1:p.Arg3924=
|
|
XM_006720726.2:c.11869A>C
|
XP_006720789.1:p.Arg3957=
|
|
XM_006720727.2:c.11626A>C
|
XP_006720790.1:p.Arg3876=
|
|
XM_011522131.1:c.11401A>C
|
XP_011520433.1:p.Arg3801=
|
|
XM_011522132.1:c.9400A>C
|
XP_011520434.1:p.Arg3134=
|
|
XM_011522133.1:c.8629A>C
|
XP_011520435.1:p.Arg2877=
|
|
XM_011522134.1:c.6001A>C
|
XP_011520436.1:p.Arg2001=
|
|
XM_005268276.5:c.11770A>C
|
XP_005268333.1:p.Arg3924=
|
|
XM_006720726.3:c.11869A>C
|
XP_006720789.1:p.Arg3957=
|
|
XM_006720727.3:c.11626A>C
|
XP_006720790.1:p.Arg3876=
|
|
XM_017022695.1:c.11770A>C
|
XP_016878184.1:p.Arg3924=
|
|
XM_017022696.1:c.11770A>C
|
XP_016878185.1:p.Arg3924=
|
|
XM_017022697.1:c.5050A>C
|
XP_016878186.1:p.Arg1684=
|
|
XM_017022698.1:c.5050A>C
|
XP_016878187.1:p.Arg1684=
|
|
NM_004667.6:c.11884A>C
MANE Select
|
NP_004658.3:p.Arg3962=
|
|