ENST00000261609.13:c.11854G>A
MANE Select
|
ENSP00000261609.8:p.Gly3952Arg
|
|
ENST00000650509.1:c.3565G>A
|
ENSP00000496936.1:p.Gly1189Arg
|
|
ENST00000261609.11:c.11854G>A
|
ENSP00000261609.7:p.Gly3952Arg
|
|
NM_004667.5:c.11854G>A
|
NP_004658.3:p.Gly3952Arg
|
|
XM_005268276.3:c.11740G>A
|
XP_005268333.1:p.Gly3914Arg
|
|
XM_005268277.3:c.11740G>A
|
XP_005268334.1:p.Gly3914Arg
|
|
XM_006720726.2:c.11839G>A
|
XP_006720789.1:p.Gly3947Arg
|
|
XM_006720727.2:c.11596G>A
|
XP_006720790.1:p.Gly3866Arg
|
|
XM_011522131.1:c.11371G>A
|
XP_011520433.1:p.Gly3791Arg
|
|
XM_011522132.1:c.9370G>A
|
XP_011520434.1:p.Gly3124Arg
|
|
XM_011522133.1:c.8599G>A
|
XP_011520435.1:p.Gly2867Arg
|
|
XM_011522134.1:c.5971G>A
|
XP_011520436.1:p.Gly1991Arg
|
|
XM_005268276.5:c.11740G>A
|
XP_005268333.1:p.Gly3914Arg
|
|
XM_006720726.3:c.11839G>A
|
XP_006720789.1:p.Gly3947Arg
|
|
XM_006720727.3:c.11596G>A
|
XP_006720790.1:p.Gly3866Arg
|
|
XM_017022695.1:c.11740G>A
|
XP_016878184.1:p.Gly3914Arg
|
|
XM_017022696.1:c.11740G>A
|
XP_016878185.1:p.Gly3914Arg
|
|
XM_017022697.1:c.5020G>A
|
XP_016878186.1:p.Gly1674Arg
|
|
XM_017022698.1:c.5020G>A
|
XP_016878187.1:p.Gly1674Arg
|
|
NM_004667.6:c.11854G>A
MANE Select
|
NP_004658.3:p.Gly3952Arg
|
|