ENST00000261609.13:c.11740A>C
MANE Select
|
ENSP00000261609.8:p.Asn3914His
|
|
ENST00000650509.1:c.3451A>C
|
ENSP00000496936.1:p.Asn1151His
|
|
ENST00000261609.11:c.11740A>C
|
ENSP00000261609.7:p.Asn3914His
|
|
ENST00000564519.1:n.255A>C
|
|
|
NM_004667.5:c.11740A>C
|
NP_004658.3:p.Asn3914His
|
|
XM_005268276.3:c.11626A>C
|
XP_005268333.1:p.Asn3876His
|
|
XM_005268277.3:c.11626A>C
|
XP_005268334.1:p.Asn3876His
|
|
XM_006720726.2:c.11725A>C
|
XP_006720789.1:p.Asn3909His
|
|
XM_006720727.2:c.11482A>C
|
XP_006720790.1:p.Asn3828His
|
|
XM_011522131.1:c.11257A>C
|
XP_011520433.1:p.Asn3753His
|
|
XM_011522132.1:c.9256A>C
|
XP_011520434.1:p.Asn3086His
|
|
XM_011522133.1:c.8485A>C
|
XP_011520435.1:p.Asn2829His
|
|
XM_011522134.1:c.5857A>C
|
XP_011520436.1:p.Asn1953His
|
|
XM_005268276.5:c.11626A>C
|
XP_005268333.1:p.Asn3876His
|
|
XM_006720726.3:c.11725A>C
|
XP_006720789.1:p.Asn3909His
|
|
XM_006720727.3:c.11482A>C
|
XP_006720790.1:p.Asn3828His
|
|
XM_017022695.1:c.11626A>C
|
XP_016878184.1:p.Asn3876His
|
|
XM_017022696.1:c.11626A>C
|
XP_016878185.1:p.Asn3876His
|
|
XM_017022697.1:c.4906A>C
|
XP_016878186.1:p.Asn1636His
|
|
XM_017022698.1:c.4906A>C
|
XP_016878187.1:p.Asn1636His
|
|
NM_004667.6:c.11740A>C
MANE Select
|
NP_004658.3:p.Asn3914His
|
|