ENST00000269980.7:c.710G>A
MANE Select
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ENSP00000269980.2:p.Gly237Asp
|
|
ENST00000269980.6:c.710G>A
|
ENSP00000269980.2:p.Gly237Asp
|
|
ENST00000457836.6:c.644G>A
|
ENSP00000416000.2:p.Gly215Asp
|
|
ENST00000535632.5:n.339G>A
|
|
|
ENST00000540732.3:c.812G>A
|
ENSP00000443246.1:p.Gly271Asp
|
|
ENST00000541315.1:c.610G>A
|
|
|
ENST00000542943.5:c.623G>A
|
ENSP00000440345.1:p.Gly208Asp
|
|
ENST00000545787.1:n.338G>A
|
|
|
ENST00000595085.5:c.710G>A
|
ENSP00000471150.2:p.Gly237Asp
|
|
NM_000709.3:c.710G>A
|
NP_000700.1:p.Gly237Asp
|
|
NM_001164783.1:c.710G>A
|
NP_001158255.1:p.Gly237Asp
|
|
NM_000709.4:c.710G>A
MANE Select
|
NP_000700.1:p.Gly237Asp
|
|
NM_001164783.2:c.710G>A
|
NP_001158255.1:p.Gly237Asp
|
|