ENST00000218099.7:c.806T>A
MANE Select
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ENSP00000218099.2:p.Val269Asp
|
|
ENST00000643157.1:n.1473T>A
|
|
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ENST00000218099.6:c.806T>A
|
ENSP00000218099.2:p.Val269Asp
|
|
ENST00000394090.2:c.692T>A
|
ENSP00000377650.2:p.Val231Asp
|
|
NM_000133.3:c.806T>A , LRG_556t1:c.806T>A
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NP_000124.1:p.Val269Asp
|
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NM_001313913.1:c.692T>A
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NP_001300842.1:p.Val231Asp
|
|
XM_005262397.3:c.677T>A
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XP_005262454.1:p.Val226Asp
|
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XM_005262397.4:c.677T>A
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XP_005262454.1:p.Val226Asp
|
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NM_000133.4:c.806T>A
MANE Select
|
NP_000124.1:p.Val269Asp
|
|
NM_001313913.2:c.692T>A
|
NP_001300842.1:p.Val231Asp
|
|