ENST00000261609.13:c.11899G>C
MANE Select
|
ENSP00000261609.8:p.Gly3967Arg
|
|
ENST00000650509.1:c.3610G>C
|
ENSP00000496936.1:p.Gly1204Arg
|
|
ENST00000261609.11:c.11899G>C
|
ENSP00000261609.7:p.Gly3967Arg
|
|
NM_004667.5:c.11899G>C
|
NP_004658.3:p.Gly3967Arg
|
|
XM_005268276.3:c.11785G>C
|
XP_005268333.1:p.Gly3929Arg
|
|
XM_005268277.3:c.11785G>C
|
XP_005268334.1:p.Gly3929Arg
|
|
XM_006720726.2:c.11884G>C
|
XP_006720789.1:p.Gly3962Arg
|
|
XM_006720727.2:c.11641G>C
|
XP_006720790.1:p.Gly3881Arg
|
|
XM_011522131.1:c.11416G>C
|
XP_011520433.1:p.Gly3806Arg
|
|
XM_011522132.1:c.9415G>C
|
XP_011520434.1:p.Gly3139Arg
|
|
XM_011522133.1:c.8644G>C
|
XP_011520435.1:p.Gly2882Arg
|
|
XM_011522134.1:c.6016G>C
|
XP_011520436.1:p.Gly2006Arg
|
|
XM_005268276.5:c.11785G>C
|
XP_005268333.1:p.Gly3929Arg
|
|
XM_006720726.3:c.11884G>C
|
XP_006720789.1:p.Gly3962Arg
|
|
XM_006720727.3:c.11641G>C
|
XP_006720790.1:p.Gly3881Arg
|
|
XM_017022695.1:c.11785G>C
|
XP_016878184.1:p.Gly3929Arg
|
|
XM_017022696.1:c.11785G>C
|
XP_016878185.1:p.Gly3929Arg
|
|
XM_017022697.1:c.5065G>C
|
XP_016878186.1:p.Gly1689Arg
|
|
XM_017022698.1:c.5065G>C
|
XP_016878187.1:p.Gly1689Arg
|
|
NM_004667.6:c.11899G>C
MANE Select
|
NP_004658.3:p.Gly3967Arg
|
|