ENST00000257904.11:c.533T>A
MANE Select
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ENSP00000257904.5:p.Leu178His
|
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ENST00000257904.10:c.533T>A
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ENSP00000257904.5:p.Leu178His
|
|
ENST00000312990.10:c.265-84T>A
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ENSP00000316889.6:n.265-84T>A
|
|
ENST00000546489.5:c.311T>A
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ENSP00000447779.1:p.Leu104His
|
|
ENST00000547281.5:c.311T>A
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ENSP00000447274.1:p.Leu104His
|
|
ENST00000549606.5:c.-157-1251T>A
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ENSP00000447005.1:n.-157-1251T>A
|
|
ENST00000550419.5:c.522+168T>A
|
ENSP00000448098.1:n.522+168T>A
|
|
ENST00000551800.5:c.311T>A
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ENSP00000449391.1:p.Leu104His
|
|
ENST00000551888.5:n.443-84T>A
|
|
|
ENST00000552254.5:c.533T>A
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ENSP00000449179.1:p.Leu178His
|
|
ENST00000553237.5:c.*172T>A
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ENSP00000448885.1:n.*172T>A
|
|
NM_000075.3:c.533T>A
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NP_000066.1:p.Leu178His
|
|
NM_000075.4:c.533T>A
MANE Select
|
NP_000066.1:p.Leu178His
|
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