ENST00000261609.13:c.11792A>T
MANE Select
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ENSP00000261609.8:p.Glu3931Val
|
|
ENST00000650509.1:c.3503A>T
|
ENSP00000496936.1:p.Glu1168Val
|
|
ENST00000261609.11:c.11792A>T
|
ENSP00000261609.7:p.Glu3931Val
|
|
ENST00000564519.1:n.307A>T
|
|
|
NM_004667.5:c.11792A>T
|
NP_004658.3:p.Glu3931Val
|
|
XM_005268276.3:c.11678A>T
|
XP_005268333.1:p.Glu3893Val
|
|
XM_005268277.3:c.11678A>T
|
XP_005268334.1:p.Glu3893Val
|
|
XM_006720726.2:c.11777A>T
|
XP_006720789.1:p.Glu3926Val
|
|
XM_006720727.2:c.11534A>T
|
XP_006720790.1:p.Glu3845Val
|
|
XM_011522131.1:c.11309A>T
|
XP_011520433.1:p.Glu3770Val
|
|
XM_011522132.1:c.9308A>T
|
XP_011520434.1:p.Glu3103Val
|
|
XM_011522133.1:c.8537A>T
|
XP_011520435.1:p.Glu2846Val
|
|
XM_011522134.1:c.5909A>T
|
XP_011520436.1:p.Glu1970Val
|
|
XM_005268276.5:c.11678A>T
|
XP_005268333.1:p.Glu3893Val
|
|
XM_006720726.3:c.11777A>T
|
XP_006720789.1:p.Glu3926Val
|
|
XM_006720727.3:c.11534A>T
|
XP_006720790.1:p.Glu3845Val
|
|
XM_017022695.1:c.11678A>T
|
XP_016878184.1:p.Glu3893Val
|
|
XM_017022696.1:c.11678A>T
|
XP_016878185.1:p.Glu3893Val
|
|
XM_017022697.1:c.4958A>T
|
XP_016878186.1:p.Glu1653Val
|
|
XM_017022698.1:c.4958A>T
|
XP_016878187.1:p.Glu1653Val
|
|
NM_004667.6:c.11792A>T
MANE Select
|
NP_004658.3:p.Glu3931Val
|
|