ENST00000261609.13:c.11912C>T
MANE Select
|
ENSP00000261609.8:p.Ala3971Val
|
|
ENST00000650509.1:c.3623C>T
|
ENSP00000496936.1:p.Ala1208Val
|
|
ENST00000261609.11:c.11912C>T
|
ENSP00000261609.7:p.Ala3971Val
|
|
NM_004667.5:c.11912C>T
|
NP_004658.3:p.Ala3971Val
|
|
XM_005268276.3:c.11798C>T
|
XP_005268333.1:p.Ala3933Val
|
|
XM_005268277.3:c.11798C>T
|
XP_005268334.1:p.Ala3933Val
|
|
XM_006720726.2:c.11897C>T
|
XP_006720789.1:p.Ala3966Val
|
|
XM_006720727.2:c.11654C>T
|
XP_006720790.1:p.Ala3885Val
|
|
XM_011522131.1:c.11429C>T
|
XP_011520433.1:p.Ala3810Val
|
|
XM_011522132.1:c.9428C>T
|
XP_011520434.1:p.Ala3143Val
|
|
XM_011522133.1:c.8657C>T
|
XP_011520435.1:p.Ala2886Val
|
|
XM_011522134.1:c.6029C>T
|
XP_011520436.1:p.Ala2010Val
|
|
XM_005268276.5:c.11798C>T
|
XP_005268333.1:p.Ala3933Val
|
|
XM_006720726.3:c.11897C>T
|
XP_006720789.1:p.Ala3966Val
|
|
XM_006720727.3:c.11654C>T
|
XP_006720790.1:p.Ala3885Val
|
|
XM_017022695.1:c.11798C>T
|
XP_016878184.1:p.Ala3933Val
|
|
XM_017022696.1:c.11798C>T
|
XP_016878185.1:p.Ala3933Val
|
|
XM_017022697.1:c.5078C>T
|
XP_016878186.1:p.Ala1693Val
|
|
XM_017022698.1:c.5078C>T
|
XP_016878187.1:p.Ala1693Val
|
|
NM_004667.6:c.11912C>T
MANE Select
|
NP_004658.3:p.Ala3971Val
|
|