ENST00000261609.13:c.11813A>C
MANE Select
|
ENSP00000261609.8:p.Asn3938Thr
|
|
ENST00000650509.1:c.3524A>C
|
ENSP00000496936.1:p.Asn1175Thr
|
|
ENST00000261609.11:c.11813A>C
|
ENSP00000261609.7:p.Asn3938Thr
|
|
NM_004667.5:c.11813A>C
|
NP_004658.3:p.Asn3938Thr
|
|
XM_005268276.3:c.11699A>C
|
XP_005268333.1:p.Asn3900Thr
|
|
XM_005268277.3:c.11699A>C
|
XP_005268334.1:p.Asn3900Thr
|
|
XM_006720726.2:c.11798A>C
|
XP_006720789.1:p.Asn3933Thr
|
|
XM_006720727.2:c.11555A>C
|
XP_006720790.1:p.Asn3852Thr
|
|
XM_011522131.1:c.11330A>C
|
XP_011520433.1:p.Asn3777Thr
|
|
XM_011522132.1:c.9329A>C
|
XP_011520434.1:p.Asn3110Thr
|
|
XM_011522133.1:c.8558A>C
|
XP_011520435.1:p.Asn2853Thr
|
|
XM_011522134.1:c.5930A>C
|
XP_011520436.1:p.Asn1977Thr
|
|
XM_005268276.5:c.11699A>C
|
XP_005268333.1:p.Asn3900Thr
|
|
XM_006720726.3:c.11798A>C
|
XP_006720789.1:p.Asn3933Thr
|
|
XM_006720727.3:c.11555A>C
|
XP_006720790.1:p.Asn3852Thr
|
|
XM_017022695.1:c.11699A>C
|
XP_016878184.1:p.Asn3900Thr
|
|
XM_017022696.1:c.11699A>C
|
XP_016878185.1:p.Asn3900Thr
|
|
XM_017022697.1:c.4979A>C
|
XP_016878186.1:p.Asn1660Thr
|
|
XM_017022698.1:c.4979A>C
|
XP_016878187.1:p.Asn1660Thr
|
|
NM_004667.6:c.11813A>C
MANE Select
|
NP_004658.3:p.Asn3938Thr
|
|