ENST00000261609.13:c.11957G>C
MANE Select
|
ENSP00000261609.8:p.Arg3986Thr
|
|
ENST00000650509.1:c.3668G>C
|
ENSP00000496936.1:p.Arg1223Thr
|
|
ENST00000261609.11:c.11957G>C
|
ENSP00000261609.7:p.Arg3986Thr
|
|
NM_004667.5:c.11957G>C
|
NP_004658.3:p.Arg3986Thr
|
|
XM_005268276.3:c.11843G>C
|
XP_005268333.1:p.Arg3948Thr
|
|
XM_005268277.3:c.11843G>C
|
XP_005268334.1:p.Arg3948Thr
|
|
XM_006720726.2:c.11942G>C
|
XP_006720789.1:p.Arg3981Thr
|
|
XM_006720727.2:c.11699G>C
|
XP_006720790.1:p.Arg3900Thr
|
|
XM_011522131.1:c.11474G>C
|
XP_011520433.1:p.Arg3825Thr
|
|
XM_011522132.1:c.9473G>C
|
XP_011520434.1:p.Arg3158Thr
|
|
XM_011522133.1:c.8702G>C
|
XP_011520435.1:p.Arg2901Thr
|
|
XM_011522134.1:c.6074G>C
|
XP_011520436.1:p.Arg2025Thr
|
|
XM_005268276.5:c.11843G>C
|
XP_005268333.1:p.Arg3948Thr
|
|
XM_006720726.3:c.11942G>C
|
XP_006720789.1:p.Arg3981Thr
|
|
XM_006720727.3:c.11699G>C
|
XP_006720790.1:p.Arg3900Thr
|
|
XM_017022695.1:c.11843G>C
|
XP_016878184.1:p.Arg3948Thr
|
|
XM_017022696.1:c.11843G>C
|
XP_016878185.1:p.Arg3948Thr
|
|
XM_017022697.1:c.5123G>C
|
XP_016878186.1:p.Arg1708Thr
|
|
XM_017022698.1:c.5123G>C
|
XP_016878187.1:p.Arg1708Thr
|
|
NM_004667.6:c.11957G>C
MANE Select
|
NP_004658.3:p.Arg3986Thr
|
|