ENST00000599672.6:c.291T>A
MANE Select
|
ENSP00000470560.1:p.Asp97Glu
|
|
ENST00000261406.7:c.273T>A
|
ENSP00000476966.2:p.Asp91Glu
|
|
ENST00000539196.2:c.154T>A
|
|
|
ENST00000599672.5:c.291T>A
|
ENSP00000470560.1:p.Asp97Glu
|
|
ENST00000607161.5:c.294T>A
|
ENSP00000480420.1:p.Asp98Glu
|
|
ENST00000611981.1:n.302T>A
|
|
|
ENST00000620255.1:n.391T>A
|
|
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NM_006331.7:c.291T>A
|
NP_006322.4:p.Asp97Glu
|
|
XM_011520907.1:c.291T>A
|
XP_011519209.1:p.Asp97Glu
|
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NM_001320049.1:c.291T>A
|
NP_001306978.1:p.Asp97Glu
|
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NR_135131.1:n.434T>A
|
|
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NM_006331.8:c.291T>A
MANE Select
|
NP_006322.4:p.Asp97Glu
|
|
NM_001320049.2:c.291T>A
|
NP_001306978.1:p.Asp97Glu
|
|
NR_135131.2:n.302T>A
|
|
|