ENST00000261609.13:c.11738A>T
MANE Select
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ENSP00000261609.8:p.Glu3913Val
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ENST00000650509.1:c.3449A>T
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ENSP00000496936.1:p.Glu1150Val
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ENST00000261609.11:c.11738A>T
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ENSP00000261609.7:p.Glu3913Val
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ENST00000564519.1:n.253A>T
|
|
|
NM_004667.5:c.11738A>T
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NP_004658.3:p.Glu3913Val
|
|
XM_005268276.3:c.11624A>T
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XP_005268333.1:p.Glu3875Val
|
|
XM_005268277.3:c.11624A>T
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XP_005268334.1:p.Glu3875Val
|
|
XM_006720726.2:c.11723A>T
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XP_006720789.1:p.Glu3908Val
|
|
XM_006720727.2:c.11480A>T
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XP_006720790.1:p.Glu3827Val
|
|
XM_011522131.1:c.11255A>T
|
XP_011520433.1:p.Glu3752Val
|
|
XM_011522132.1:c.9254A>T
|
XP_011520434.1:p.Glu3085Val
|
|
XM_011522133.1:c.8483A>T
|
XP_011520435.1:p.Glu2828Val
|
|
XM_011522134.1:c.5855A>T
|
XP_011520436.1:p.Glu1952Val
|
|
XM_005268276.5:c.11624A>T
|
XP_005268333.1:p.Glu3875Val
|
|
XM_006720726.3:c.11723A>T
|
XP_006720789.1:p.Glu3908Val
|
|
XM_006720727.3:c.11480A>T
|
XP_006720790.1:p.Glu3827Val
|
|
XM_017022695.1:c.11624A>T
|
XP_016878184.1:p.Glu3875Val
|
|
XM_017022696.1:c.11624A>T
|
XP_016878185.1:p.Glu3875Val
|
|
XM_017022697.1:c.4904A>T
|
XP_016878186.1:p.Glu1635Val
|
|
XM_017022698.1:c.4904A>T
|
XP_016878187.1:p.Glu1635Val
|
|
NM_004667.6:c.11738A>T
MANE Select
|
NP_004658.3:p.Glu3913Val
|
|