ENST00000261609.13:c.11740A>T
MANE Select
|
ENSP00000261609.8:p.Asn3914Tyr
|
|
ENST00000650509.1:c.3451A>T
|
ENSP00000496936.1:p.Asn1151Tyr
|
|
ENST00000261609.11:c.11740A>T
|
ENSP00000261609.7:p.Asn3914Tyr
|
|
ENST00000564519.1:n.255A>T
|
|
|
NM_004667.5:c.11740A>T
|
NP_004658.3:p.Asn3914Tyr
|
|
XM_005268276.3:c.11626A>T
|
XP_005268333.1:p.Asn3876Tyr
|
|
XM_005268277.3:c.11626A>T
|
XP_005268334.1:p.Asn3876Tyr
|
|
XM_006720726.2:c.11725A>T
|
XP_006720789.1:p.Asn3909Tyr
|
|
XM_006720727.2:c.11482A>T
|
XP_006720790.1:p.Asn3828Tyr
|
|
XM_011522131.1:c.11257A>T
|
XP_011520433.1:p.Asn3753Tyr
|
|
XM_011522132.1:c.9256A>T
|
XP_011520434.1:p.Asn3086Tyr
|
|
XM_011522133.1:c.8485A>T
|
XP_011520435.1:p.Asn2829Tyr
|
|
XM_011522134.1:c.5857A>T
|
XP_011520436.1:p.Asn1953Tyr
|
|
XM_005268276.5:c.11626A>T
|
XP_005268333.1:p.Asn3876Tyr
|
|
XM_006720726.3:c.11725A>T
|
XP_006720789.1:p.Asn3909Tyr
|
|
XM_006720727.3:c.11482A>T
|
XP_006720790.1:p.Asn3828Tyr
|
|
XM_017022695.1:c.11626A>T
|
XP_016878184.1:p.Asn3876Tyr
|
|
XM_017022696.1:c.11626A>T
|
XP_016878185.1:p.Asn3876Tyr
|
|
XM_017022697.1:c.4906A>T
|
XP_016878186.1:p.Asn1636Tyr
|
|
XM_017022698.1:c.4906A>T
|
XP_016878187.1:p.Asn1636Tyr
|
|
NM_004667.6:c.11740A>T
MANE Select
|
NP_004658.3:p.Asn3914Tyr
|
|