ENST00000452035.7:n.2055T>A
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|
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ENST00000483004.2:c.1447T>A
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ENSP00000419887.2:p.Phe483Ile
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ENST00000698628.1:c.1624+254T>A
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ENSP00000513848.1:n.1624+254T>A
|
|
ENST00000698629.1:n.1840T>A
|
|
|
ENST00000698630.1:n.2379T>A
|
|
|
ENST00000698631.1:n.2380T>A
|
|
|
ENST00000698632.1:n.3174T>A
|
|
|
ENST00000698633.1:n.3064T>A
|
|
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ENST00000698636.1:n.1885T>A
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|
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ENST00000425368.7:c.1663T>A
MANE Select
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ENSP00000416561.2:p.Phe555Ile
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|
ENST00000425368.6:c.1663T>A
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ENSP00000416561.2:p.Phe555Ile
|
|
ENST00000456570.5:c.3169T>A
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ENSP00000410815.1:p.Phe1057Ile
|
|
ENST00000467360.1:n.789T>A
|
|
|
ENST00000477310.1:c.2716T>A
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ENSP00000418996.1:p.Phe906Ile
|
|
ENST00000483004.1:c.285T>A
|
|
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NM_001710.5:c.1663T>A , LRG_136t1:c.1663T>A
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NP_001701.2:p.Phe555Ile
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NM_001710.6:c.1663T>A
MANE Select
|
NP_001701.2:p.Phe555Ile
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