ENST00000261609.13:c.11789A>T
MANE Select
|
ENSP00000261609.8:p.Asp3930Val
|
|
ENST00000650509.1:c.3500A>T
|
ENSP00000496936.1:p.Asp1167Val
|
|
ENST00000261609.11:c.11789A>T
|
ENSP00000261609.7:p.Asp3930Val
|
|
ENST00000564519.1:n.304A>T
|
|
|
NM_004667.5:c.11789A>T
|
NP_004658.3:p.Asp3930Val
|
|
XM_005268276.3:c.11675A>T
|
XP_005268333.1:p.Asp3892Val
|
|
XM_005268277.3:c.11675A>T
|
XP_005268334.1:p.Asp3892Val
|
|
XM_006720726.2:c.11774A>T
|
XP_006720789.1:p.Asp3925Val
|
|
XM_006720727.2:c.11531A>T
|
XP_006720790.1:p.Asp3844Val
|
|
XM_011522131.1:c.11306A>T
|
XP_011520433.1:p.Asp3769Val
|
|
XM_011522132.1:c.9305A>T
|
XP_011520434.1:p.Asp3102Val
|
|
XM_011522133.1:c.8534A>T
|
XP_011520435.1:p.Asp2845Val
|
|
XM_011522134.1:c.5906A>T
|
XP_011520436.1:p.Asp1969Val
|
|
XM_005268276.5:c.11675A>T
|
XP_005268333.1:p.Asp3892Val
|
|
XM_006720726.3:c.11774A>T
|
XP_006720789.1:p.Asp3925Val
|
|
XM_006720727.3:c.11531A>T
|
XP_006720790.1:p.Asp3844Val
|
|
XM_017022695.1:c.11675A>T
|
XP_016878184.1:p.Asp3892Val
|
|
XM_017022696.1:c.11675A>T
|
XP_016878185.1:p.Asp3892Val
|
|
XM_017022697.1:c.4955A>T
|
XP_016878186.1:p.Asp1652Val
|
|
XM_017022698.1:c.4955A>T
|
XP_016878187.1:p.Asp1652Val
|
|
NM_004667.6:c.11789A>T
MANE Select
|
NP_004658.3:p.Asp3930Val
|
|