ENST00000261609.13:c.11740A>G
MANE Select
|
ENSP00000261609.8:p.Asn3914Asp
|
|
ENST00000650509.1:c.3451A>G
|
ENSP00000496936.1:p.Asn1151Asp
|
|
ENST00000261609.11:c.11740A>G
|
ENSP00000261609.7:p.Asn3914Asp
|
|
ENST00000564519.1:n.255A>G
|
|
|
NM_004667.5:c.11740A>G
|
NP_004658.3:p.Asn3914Asp
|
|
XM_005268276.3:c.11626A>G
|
XP_005268333.1:p.Asn3876Asp
|
|
XM_005268277.3:c.11626A>G
|
XP_005268334.1:p.Asn3876Asp
|
|
XM_006720726.2:c.11725A>G
|
XP_006720789.1:p.Asn3909Asp
|
|
XM_006720727.2:c.11482A>G
|
XP_006720790.1:p.Asn3828Asp
|
|
XM_011522131.1:c.11257A>G
|
XP_011520433.1:p.Asn3753Asp
|
|
XM_011522132.1:c.9256A>G
|
XP_011520434.1:p.Asn3086Asp
|
|
XM_011522133.1:c.8485A>G
|
XP_011520435.1:p.Asn2829Asp
|
|
XM_011522134.1:c.5857A>G
|
XP_011520436.1:p.Asn1953Asp
|
|
XM_005268276.5:c.11626A>G
|
XP_005268333.1:p.Asn3876Asp
|
|
XM_006720726.3:c.11725A>G
|
XP_006720789.1:p.Asn3909Asp
|
|
XM_006720727.3:c.11482A>G
|
XP_006720790.1:p.Asn3828Asp
|
|
XM_017022695.1:c.11626A>G
|
XP_016878184.1:p.Asn3876Asp
|
|
XM_017022696.1:c.11626A>G
|
XP_016878185.1:p.Asn3876Asp
|
|
XM_017022697.1:c.4906A>G
|
XP_016878186.1:p.Asn1636Asp
|
|
XM_017022698.1:c.4906A>G
|
XP_016878187.1:p.Asn1636Asp
|
|
NM_004667.6:c.11740A>G
MANE Select
|
NP_004658.3:p.Asn3914Asp
|
|