ENST00000218099.7:c.681T>A
MANE Select
|
ENSP00000218099.2:p.Val227=
|
|
ENST00000643157.1:n.1348T>A
|
|
|
ENST00000218099.6:c.681T>A
|
ENSP00000218099.2:p.Val227=
|
|
ENST00000394090.2:c.567T>A
|
ENSP00000377650.2:p.Val189=
|
|
NM_000133.3:c.681T>A , LRG_556t1:c.681T>A
|
NP_000124.1:p.Val227=
|
|
NM_001313913.1:c.567T>A
|
NP_001300842.1:p.Val189=
|
|
XM_005262397.3:c.552T>A
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XP_005262454.1:p.Val184=
|
|
XM_005262397.4:c.552T>A
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XP_005262454.1:p.Val184=
|
|
NM_000133.4:c.681T>A
MANE Select
|
NP_000124.1:p.Val227=
|
|
NM_001313913.2:c.567T>A
|
NP_001300842.1:p.Val189=
|
|