ENST00000426263.10:c.355T>A
MANE Select
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ENSP00000416293.2:p.Phe119Ile
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|
ENST00000674765.1:c.355T>A
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ENSP00000501811.1:p.Phe119Ile
|
|
ENST00000675112.1:n.378T>A
|
|
|
ENST00000676254.1:n.804T>A
|
|
|
ENST00000372500.4:c.259T>A
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ENSP00000361578.4:p.Phe87Ile
|
|
ENST00000426263.7:c.355T>A
|
ENSP00000416293.2:p.Phe119Ile
|
|
ENST00000439722.2:c.234T>A
|
ENSP00000395521.2:n.234T>A
|
|
ENST00000475162.3:c.254T>A
|
|
|
ENST00000625233.2:n.563T>A
|
|
|
ENST00000630287.2:c.355T>A
|
ENSP00000486694.1:p.Phe119Ile
|
|
NM_006516.2:c.355T>A
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NP_006507.2:p.Phe119Ile
|
|
NM_006516.3:c.355T>A
|
NP_006507.2:p.Phe119Ile
|
|
NM_006516.4:c.355T>A
MANE Select
|
NP_006507.2:p.Phe119Ile
|
|