ENST00000261609.13:c.11720A>T
MANE Select
|
ENSP00000261609.8:p.Glu3907Val
|
|
ENST00000650509.1:c.3431A>T
|
ENSP00000496936.1:p.Glu1144Val
|
|
ENST00000261609.11:c.11720A>T
|
ENSP00000261609.7:p.Glu3907Val
|
|
ENST00000564519.1:n.235A>T
|
|
|
NM_004667.5:c.11720A>T
|
NP_004658.3:p.Glu3907Val
|
|
XM_005268276.3:c.11606A>T
|
XP_005268333.1:p.Glu3869Val
|
|
XM_005268277.3:c.11606A>T
|
XP_005268334.1:p.Glu3869Val
|
|
XM_006720726.2:c.11705A>T
|
XP_006720789.1:p.Glu3902Val
|
|
XM_006720727.2:c.11462A>T
|
XP_006720790.1:p.Glu3821Val
|
|
XM_011522131.1:c.11237A>T
|
XP_011520433.1:p.Glu3746Val
|
|
XM_011522132.1:c.9236A>T
|
XP_011520434.1:p.Glu3079Val
|
|
XM_011522133.1:c.8465A>T
|
XP_011520435.1:p.Glu2822Val
|
|
XM_011522134.1:c.5837A>T
|
XP_011520436.1:p.Glu1946Val
|
|
XM_005268276.5:c.11606A>T
|
XP_005268333.1:p.Glu3869Val
|
|
XM_006720726.3:c.11705A>T
|
XP_006720789.1:p.Glu3902Val
|
|
XM_006720727.3:c.11462A>T
|
XP_006720790.1:p.Glu3821Val
|
|
XM_017022695.1:c.11606A>T
|
XP_016878184.1:p.Glu3869Val
|
|
XM_017022696.1:c.11606A>T
|
XP_016878185.1:p.Glu3869Val
|
|
XM_017022697.1:c.4886A>T
|
XP_016878186.1:p.Glu1629Val
|
|
XM_017022698.1:c.4886A>T
|
XP_016878187.1:p.Glu1629Val
|
|
NM_004667.6:c.11720A>T
MANE Select
|
NP_004658.3:p.Glu3907Val
|
|