ENST00000346342.8:c.325T>A
MANE Select
|
ENSP00000329546.4:p.Phe109Ile
|
|
ENST00000346342.7:c.325T>A
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ENSP00000329546.3:p.Phe109Ile
|
|
ENST00000375581.3:c.391T>A
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ENSP00000364731.3:p.Phe131Ile
|
|
ENST00000444337.1:c.*133T>A
|
ENSP00000387669.1:n.*133T>A
|
|
ENST00000473085.1:n.272T>A
|
|
|
ENST00000479674.1:n.658T>A
|
|
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ENST00000541084.5:c.139T>A
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ENSP00000442051.2:p.Phe47Ile
|
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NM_000131.4:c.391T>A , LRG_554t1:c.391T>A
|
NP_000122.1:p.Phe131Ile
|
|
NM_001267554.1:c.139T>A
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NP_001254483.1:p.Phe47Ile
|
|
NM_019616.3:c.325T>A , LRG_554t2:c.325T>A
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NP_062562.1:p.Phe109Ile
|
|
NR_051961.1:n.412T>A
|
|
|
XM_006719963.2:c.325T>A
|
XP_006720026.1:p.Phe109Ile
|
|
XM_011537474.1:c.325T>A
|
XP_011535776.1:p.Phe109Ile
|
|
XM_011537475.1:c.139T>A
|
XP_011535777.1:p.Phe47Ile
|
|
XM_011537477.1:c.286T>A
|
XP_011535779.1:p.Phe96Ile
|
|
XM_006719963.3:c.370T>A
|
XP_006720026.2:p.Phe124Ile
|
|
XM_011537474.2:c.370T>A
|
XP_011535776.2:p.Phe124Ile
|
|
XM_011537475.2:c.184T>A
|
XP_011535777.2:p.Phe62Ile
|
|
NM_019616.4:c.325T>A
MANE Select
|
NP_062562.1:p.Phe109Ile
|
|
NR_051961.2:n.409T>A
|
|
|
NM_001267554.2:c.139T>A
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NP_001254483.1:p.Phe47Ile
|
|