ENST00000258781.11:c.328G>T
MANE Select
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ENSP00000258781.7:p.Asp110Tyr
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ENST00000648329.1:c.328G>T
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ENSP00000496916.1:p.Asp110Tyr
|
|
ENST00000258781.10:c.328G>T
|
ENSP00000258781.6:p.Asp110Tyr
|
|
ENST00000381112.7:c.391G>T
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ENSP00000370503.3:p.Asp131Tyr
|
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ENST00000461377.5:n.681G>T
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|
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ENST00000472223.5:n.395G>T
|
|
|
ENST00000474617.1:c.310G>T
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ENSP00000419474.1:p.Asp104Tyr
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|
ENST00000475551.5:c.310G>T
|
ENSP00000417180.1:p.Asp104Tyr
|
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ENST00000476594.1:n.413G>T
|
|
|
ENST00000478582.5:n.539G>T
|
|
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ENST00000480658.5:n.301-3941G>T
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|
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ENST00000482714.5:n.250G>T
|
|
|
ENST00000488727.5:c.328G>T
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ENSP00000417251.1:p.Asp110Tyr
|
|
ENST00000492883.5:n.340G>T
|
|
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ENST00000541586.5:c.154G>T
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ENSP00000444725.1:p.Asp52Tyr
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|
ENST00000544363.5:c.328G>T
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ENSP00000438035.1:p.Asp110Tyr
|
|
NM_001029835.2:c.391G>T , LRG_664t1:c.391G>T
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NP_001025006.1:p.Asp131Tyr
|
|
NM_001167934.1:c.154G>T
|
NP_001161406.1:p.Asp52Tyr
|
|
NM_001167935.1:c.328G>T
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NP_001161407.1:p.Asp110Tyr
|
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NM_031443.3:c.328G>T , LRG_664t2:c.328G>T
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NP_113631.1:p.Asp110Tyr
|
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NR_030770.1:n.410G>T
|
|
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XM_006715785.2:c.217G>T
|
XP_006715848.1:p.Asp73Tyr
|
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XM_006715786.2:c.391G>T
|
XP_006715849.1:p.Asp131Tyr
|
|
XM_011515561.1:c.391G>T
|
XP_011513863.1:p.Asp131Tyr
|
|
XM_011515562.1:c.328G>T
|
XP_011513864.1:p.Asp110Tyr
|
|
XM_011515563.1:c.217G>T
|
XP_011513865.1:p.Asp73Tyr
|
|
XM_011515564.1:c.154G>T
|
XP_011513866.1:p.Asp52Tyr
|
|
XR_428088.2:n.404G>T
|
|
|
NM_001363458.1:c.328G>T
|
NP_001350387.1:p.Asp110Tyr
|
|
NM_001363459.1:c.154G>T
|
NP_001350388.1:p.Asp52Tyr
|
|
XM_006715785.4:c.217G>T
|
XP_006715848.1:p.Asp73Tyr
|
|
XM_006715786.3:c.391G>T
|
XP_006715849.1:p.Asp131Tyr
|
|
XM_011515561.2:c.391G>T
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XP_011513863.1:p.Asp131Tyr
|
|
XM_011515563.3:c.217G>T
|
XP_011513865.1:p.Asp73Tyr
|
|
XM_017012671.1:c.391G>T
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XP_016868160.1:p.Asp131Tyr
|
|
XM_017012672.2:c.217G>T
|
XP_016868161.1:p.Asp73Tyr
|
|
XM_017012673.1:c.154G>T
|
XP_016868162.1:p.Asp52Tyr
|
|
XR_428088.3:n.424G>T
|
|
|
NM_001363458.2:c.328G>T
|
NP_001350387.1:p.Asp110Tyr
|
|
NM_001363459.2:c.154G>T
|
NP_001350388.1:p.Asp52Tyr
|
|
NM_031443.4:c.328G>T
MANE Select
|
NP_113631.1:p.Asp110Tyr
|
|
NR_030770.2:n.410G>T
|
|
|
NM_001167934.2:c.154G>T
|
NP_001161406.1:p.Asp52Tyr
|
|
NM_001167935.2:c.328G>T
|
NP_001161407.1:p.Asp110Tyr
|
|