ENST00000578493.2:n.1024C>A
|
|
|
ENST00000699291.1:c.816C>A
|
ENSP00000514272.1:n.816C>A
|
|
ENST00000699292.1:n.1226C>A
|
|
|
ENST00000225275.4:c.1691C>A
MANE Select
|
ENSP00000225275.3:p.Ala564Glu
|
|
ENST00000225275.3:c.1691C>A
|
ENSP00000225275.3:p.Ala564Glu
|
|
ENST00000577220.1:c.149C>A
|
ENSP00000464668.1:p.Ala50Glu
|
|
NM_000250.1:c.1691C>A , LRG_84t1:c.1691C>A
|
NP_000241.1:p.Ala564Glu
|
|
XM_011524821.1:c.1877C>A
|
XP_011523123.1:p.Ala626Glu
|
|
XM_011524822.1:c.1406C>A
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XP_011523124.1:p.Ala469Glu
|
|
NM_000250.2:c.1691C>A
MANE Select
|
NP_000241.1:p.Ala564Glu
|
|