ENST00000452035.7:n.2116A>T
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|
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ENST00000483004.2:c.1508A>T
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ENSP00000419887.2:p.Tyr503Phe
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ENST00000698628.1:c.1624+315A>T
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ENSP00000513848.1:n.1624+315A>T
|
|
ENST00000698629.1:n.1901A>T
|
|
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ENST00000698630.1:n.2440A>T
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ENST00000698631.1:n.2441A>T
|
|
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ENST00000698632.1:n.3235A>T
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|
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ENST00000698633.1:n.3125A>T
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|
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ENST00000698636.1:n.1946A>T
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|
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ENST00000425368.7:c.1724A>T
MANE Select
|
ENSP00000416561.2:p.Tyr575Phe
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|
ENST00000425368.6:c.1724A>T
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ENSP00000416561.2:p.Tyr575Phe
|
|
ENST00000456570.5:c.3230A>T
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ENSP00000410815.1:p.Tyr1077Phe
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|
ENST00000467360.1:n.850A>T
|
|
|
ENST00000477310.1:c.2777A>T
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ENSP00000418996.1:p.Tyr926Phe
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ENST00000483004.1:c.346A>T
|
|
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NM_001710.5:c.1724A>T , LRG_136t1:c.1724A>T
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NP_001701.2:p.Tyr575Phe
|
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NM_001710.6:c.1724A>T
MANE Select
|
NP_001701.2:p.Tyr575Phe
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