ENST00000261609.13:c.11785C=
MANE Select
|
ENSP00000261609.8:p.Gln3929=
|
|
ENST00000650509.1:c.3496C=
|
ENSP00000496936.1:p.Gln1166=
|
|
ENST00000261609.11:c.11785C=
|
ENSP00000261609.7:p.Gln3929=
|
|
ENST00000564519.1:n.300C=
|
|
|
NM_004667.5:c.11785C=
|
NP_004658.3:p.Gln3929=
|
|
XM_005268276.3:c.11671C=
|
XP_005268333.1:p.Gln3891=
|
|
XM_005268277.3:c.11671C=
|
XP_005268334.1:p.Gln3891=
|
|
XM_006720726.2:c.11770C=
|
XP_006720789.1:p.Gln3924=
|
|
XM_006720727.2:c.11527C=
|
XP_006720790.1:p.Gln3843=
|
|
XM_011522131.1:c.11302C=
|
XP_011520433.1:p.Gln3768=
|
|
XM_011522132.1:c.9301C=
|
XP_011520434.1:p.Gln3101=
|
|
XM_011522133.1:c.8530C=
|
XP_011520435.1:p.Gln2844=
|
|
XM_011522134.1:c.5902C=
|
XP_011520436.1:p.Gln1968=
|
|
XM_005268276.5:c.11671C=
|
XP_005268333.1:p.Gln3891=
|
|
XM_006720726.3:c.11770C=
|
XP_006720789.1:p.Gln3924=
|
|
XM_006720727.3:c.11527C=
|
XP_006720790.1:p.Gln3843=
|
|
XM_017022695.1:c.11671C=
|
XP_016878184.1:p.Gln3891=
|
|
XM_017022696.1:c.11671C=
|
XP_016878185.1:p.Gln3891=
|
|
XM_017022697.1:c.4951C=
|
XP_016878186.1:p.Gln1651=
|
|
XM_017022698.1:c.4951C=
|
XP_016878187.1:p.Gln1651=
|
|
NM_004667.6:c.11785C=
MANE Select
|
NP_004658.3:p.Gln3929=
|
|