ENST00000261609.13:c.11742C>G
MANE Select
|
ENSP00000261609.8:p.Asn3914Lys
|
|
ENST00000650509.1:c.3453C>G
|
ENSP00000496936.1:p.Asn1151Lys
|
|
ENST00000261609.11:c.11742C>G
|
ENSP00000261609.7:p.Asn3914Lys
|
|
ENST00000564519.1:n.257C>G
|
|
|
NM_004667.5:c.11742C>G
|
NP_004658.3:p.Asn3914Lys
|
|
XM_005268276.3:c.11628C>G
|
XP_005268333.1:p.Asn3876Lys
|
|
XM_005268277.3:c.11628C>G
|
XP_005268334.1:p.Asn3876Lys
|
|
XM_006720726.2:c.11727C>G
|
XP_006720789.1:p.Asn3909Lys
|
|
XM_006720727.2:c.11484C>G
|
XP_006720790.1:p.Asn3828Lys
|
|
XM_011522131.1:c.11259C>G
|
XP_011520433.1:p.Asn3753Lys
|
|
XM_011522132.1:c.9258C>G
|
XP_011520434.1:p.Asn3086Lys
|
|
XM_011522133.1:c.8487C>G
|
XP_011520435.1:p.Asn2829Lys
|
|
XM_011522134.1:c.5859C>G
|
XP_011520436.1:p.Asn1953Lys
|
|
XM_005268276.5:c.11628C>G
|
XP_005268333.1:p.Asn3876Lys
|
|
XM_006720726.3:c.11727C>G
|
XP_006720789.1:p.Asn3909Lys
|
|
XM_006720727.3:c.11484C>G
|
XP_006720790.1:p.Asn3828Lys
|
|
XM_017022695.1:c.11628C>G
|
XP_016878184.1:p.Asn3876Lys
|
|
XM_017022696.1:c.11628C>G
|
XP_016878185.1:p.Asn3876Lys
|
|
XM_017022697.1:c.4908C>G
|
XP_016878186.1:p.Asn1636Lys
|
|
XM_017022698.1:c.4908C>G
|
XP_016878187.1:p.Asn1636Lys
|
|
NM_004667.6:c.11742C>G
MANE Select
|
NP_004658.3:p.Asn3914Lys
|
|