ENST00000261609.13:c.12012G>T
MANE Select
|
ENSP00000261609.8:p.Gly4004=
|
|
ENST00000650509.1:c.3723G>T
|
ENSP00000496936.1:p.Gly1241=
|
|
ENST00000261609.11:c.12012G>T
|
ENSP00000261609.7:p.Gly4004=
|
|
NM_004667.5:c.12012G>T
|
NP_004658.3:p.Gly4004=
|
|
XM_005268276.3:c.11898G>T
|
XP_005268333.1:p.Gly3966=
|
|
XM_005268277.3:c.11898G>T
|
XP_005268334.1:p.Gly3966=
|
|
XM_006720726.2:c.11997G>T
|
XP_006720789.1:p.Gly3999=
|
|
XM_006720727.2:c.11754G>T
|
XP_006720790.1:p.Gly3918=
|
|
XM_011522131.1:c.11529G>T
|
XP_011520433.1:p.Gly3843=
|
|
XM_011522132.1:c.9528G>T
|
XP_011520434.1:p.Gly3176=
|
|
XM_011522133.1:c.8757G>T
|
XP_011520435.1:p.Gly2919=
|
|
XM_011522134.1:c.6129G>T
|
XP_011520436.1:p.Gly2043=
|
|
XM_005268276.5:c.11898G>T
|
XP_005268333.1:p.Gly3966=
|
|
XM_006720726.3:c.11997G>T
|
XP_006720789.1:p.Gly3999=
|
|
XM_006720727.3:c.11754G>T
|
XP_006720790.1:p.Gly3918=
|
|
XM_017022695.1:c.11898G>T
|
XP_016878184.1:p.Gly3966=
|
|
XM_017022696.1:c.11898G>T
|
XP_016878185.1:p.Gly3966=
|
|
XM_017022697.1:c.5178G>T
|
XP_016878186.1:p.Gly1726=
|
|
XM_017022698.1:c.5178G>T
|
XP_016878187.1:p.Gly1726=
|
|
NM_004667.6:c.12012G>T
MANE Select
|
NP_004658.3:p.Gly4004=
|
|