ENST00000261609.13:c.11769C>G
MANE Select
|
ENSP00000261609.8:p.Asp3923Glu
|
|
ENST00000650509.1:c.3480C>G
|
ENSP00000496936.1:p.Asp1160Glu
|
|
ENST00000261609.11:c.11769C>G
|
ENSP00000261609.7:p.Asp3923Glu
|
|
ENST00000564519.1:n.284C>G
|
|
|
NM_004667.5:c.11769C>G
|
NP_004658.3:p.Asp3923Glu
|
|
XM_005268276.3:c.11655C>G
|
XP_005268333.1:p.Asp3885Glu
|
|
XM_005268277.3:c.11655C>G
|
XP_005268334.1:p.Asp3885Glu
|
|
XM_006720726.2:c.11754C>G
|
XP_006720789.1:p.Asp3918Glu
|
|
XM_006720727.2:c.11511C>G
|
XP_006720790.1:p.Asp3837Glu
|
|
XM_011522131.1:c.11286C>G
|
XP_011520433.1:p.Asp3762Glu
|
|
XM_011522132.1:c.9285C>G
|
XP_011520434.1:p.Asp3095Glu
|
|
XM_011522133.1:c.8514C>G
|
XP_011520435.1:p.Asp2838Glu
|
|
XM_011522134.1:c.5886C>G
|
XP_011520436.1:p.Asp1962Glu
|
|
XM_005268276.5:c.11655C>G
|
XP_005268333.1:p.Asp3885Glu
|
|
XM_006720726.3:c.11754C>G
|
XP_006720789.1:p.Asp3918Glu
|
|
XM_006720727.3:c.11511C>G
|
XP_006720790.1:p.Asp3837Glu
|
|
XM_017022695.1:c.11655C>G
|
XP_016878184.1:p.Asp3885Glu
|
|
XM_017022696.1:c.11655C>G
|
XP_016878185.1:p.Asp3885Glu
|
|
XM_017022697.1:c.4935C>G
|
XP_016878186.1:p.Asp1645Glu
|
|
XM_017022698.1:c.4935C>G
|
XP_016878187.1:p.Asp1645Glu
|
|
NM_004667.6:c.11769C>G
MANE Select
|
NP_004658.3:p.Asp3923Glu
|
|