ENST00000261609.13:c.11909G>T
MANE Select
|
ENSP00000261609.8:p.Gly3970Val
|
|
ENST00000650509.1:c.3620G>T
|
ENSP00000496936.1:p.Gly1207Val
|
|
ENST00000261609.11:c.11909G>T
|
ENSP00000261609.7:p.Gly3970Val
|
|
NM_004667.5:c.11909G>T
|
NP_004658.3:p.Gly3970Val
|
|
XM_005268276.3:c.11795G>T
|
XP_005268333.1:p.Gly3932Val
|
|
XM_005268277.3:c.11795G>T
|
XP_005268334.1:p.Gly3932Val
|
|
XM_006720726.2:c.11894G>T
|
XP_006720789.1:p.Gly3965Val
|
|
XM_006720727.2:c.11651G>T
|
XP_006720790.1:p.Gly3884Val
|
|
XM_011522131.1:c.11426G>T
|
XP_011520433.1:p.Gly3809Val
|
|
XM_011522132.1:c.9425G>T
|
XP_011520434.1:p.Gly3142Val
|
|
XM_011522133.1:c.8654G>T
|
XP_011520435.1:p.Gly2885Val
|
|
XM_011522134.1:c.6026G>T
|
XP_011520436.1:p.Gly2009Val
|
|
XM_005268276.5:c.11795G>T
|
XP_005268333.1:p.Gly3932Val
|
|
XM_006720726.3:c.11894G>T
|
XP_006720789.1:p.Gly3965Val
|
|
XM_006720727.3:c.11651G>T
|
XP_006720790.1:p.Gly3884Val
|
|
XM_017022695.1:c.11795G>T
|
XP_016878184.1:p.Gly3932Val
|
|
XM_017022696.1:c.11795G>T
|
XP_016878185.1:p.Gly3932Val
|
|
XM_017022697.1:c.5075G>T
|
XP_016878186.1:p.Gly1692Val
|
|
XM_017022698.1:c.5075G>T
|
XP_016878187.1:p.Gly1692Val
|
|
NM_004667.6:c.11909G>T
MANE Select
|
NP_004658.3:p.Gly3970Val
|
|