ENST00000261609.13:c.11741A>C
MANE Select
|
ENSP00000261609.8:p.Asn3914Thr
|
|
ENST00000650509.1:c.3452A>C
|
ENSP00000496936.1:p.Asn1151Thr
|
|
ENST00000261609.11:c.11741A>C
|
ENSP00000261609.7:p.Asn3914Thr
|
|
ENST00000564519.1:n.256A>C
|
|
|
NM_004667.5:c.11741A>C
|
NP_004658.3:p.Asn3914Thr
|
|
XM_005268276.3:c.11627A>C
|
XP_005268333.1:p.Asn3876Thr
|
|
XM_005268277.3:c.11627A>C
|
XP_005268334.1:p.Asn3876Thr
|
|
XM_006720726.2:c.11726A>C
|
XP_006720789.1:p.Asn3909Thr
|
|
XM_006720727.2:c.11483A>C
|
XP_006720790.1:p.Asn3828Thr
|
|
XM_011522131.1:c.11258A>C
|
XP_011520433.1:p.Asn3753Thr
|
|
XM_011522132.1:c.9257A>C
|
XP_011520434.1:p.Asn3086Thr
|
|
XM_011522133.1:c.8486A>C
|
XP_011520435.1:p.Asn2829Thr
|
|
XM_011522134.1:c.5858A>C
|
XP_011520436.1:p.Asn1953Thr
|
|
XM_005268276.5:c.11627A>C
|
XP_005268333.1:p.Asn3876Thr
|
|
XM_006720726.3:c.11726A>C
|
XP_006720789.1:p.Asn3909Thr
|
|
XM_006720727.3:c.11483A>C
|
XP_006720790.1:p.Asn3828Thr
|
|
XM_017022695.1:c.11627A>C
|
XP_016878184.1:p.Asn3876Thr
|
|
XM_017022696.1:c.11627A>C
|
XP_016878185.1:p.Asn3876Thr
|
|
XM_017022697.1:c.4907A>C
|
XP_016878186.1:p.Asn1636Thr
|
|
XM_017022698.1:c.4907A>C
|
XP_016878187.1:p.Asn1636Thr
|
|
NM_004667.6:c.11741A>C
MANE Select
|
NP_004658.3:p.Asn3914Thr
|
|