ENST00000261609.13:c.11768A>T
MANE Select
|
ENSP00000261609.8:p.Asp3923Val
|
|
ENST00000650509.1:c.3479A>T
|
ENSP00000496936.1:p.Asp1160Val
|
|
ENST00000261609.11:c.11768A>T
|
ENSP00000261609.7:p.Asp3923Val
|
|
ENST00000564519.1:n.283A>T
|
|
|
NM_004667.5:c.11768A>T
|
NP_004658.3:p.Asp3923Val
|
|
XM_005268276.3:c.11654A>T
|
XP_005268333.1:p.Asp3885Val
|
|
XM_005268277.3:c.11654A>T
|
XP_005268334.1:p.Asp3885Val
|
|
XM_006720726.2:c.11753A>T
|
XP_006720789.1:p.Asp3918Val
|
|
XM_006720727.2:c.11510A>T
|
XP_006720790.1:p.Asp3837Val
|
|
XM_011522131.1:c.11285A>T
|
XP_011520433.1:p.Asp3762Val
|
|
XM_011522132.1:c.9284A>T
|
XP_011520434.1:p.Asp3095Val
|
|
XM_011522133.1:c.8513A>T
|
XP_011520435.1:p.Asp2838Val
|
|
XM_011522134.1:c.5885A>T
|
XP_011520436.1:p.Asp1962Val
|
|
XM_005268276.5:c.11654A>T
|
XP_005268333.1:p.Asp3885Val
|
|
XM_006720726.3:c.11753A>T
|
XP_006720789.1:p.Asp3918Val
|
|
XM_006720727.3:c.11510A>T
|
XP_006720790.1:p.Asp3837Val
|
|
XM_017022695.1:c.11654A>T
|
XP_016878184.1:p.Asp3885Val
|
|
XM_017022696.1:c.11654A>T
|
XP_016878185.1:p.Asp3885Val
|
|
XM_017022697.1:c.4934A>T
|
XP_016878186.1:p.Asp1645Val
|
|
XM_017022698.1:c.4934A>T
|
XP_016878187.1:p.Asp1645Val
|
|
NM_004667.6:c.11768A>T
MANE Select
|
NP_004658.3:p.Asp3923Val
|
|