ENST00000452035.7:n.2331G>T
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|
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ENST00000483004.2:c.1628G>T
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ENSP00000419887.2:p.Cys543Phe
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ENST00000698628.1:c.1625-211G>T
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ENSP00000513848.1:n.1625-211G>T
|
|
ENST00000698629.1:n.2116G>T
|
|
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ENST00000698630.1:n.2560G>T
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|
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ENST00000698631.1:n.2561G>T
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|
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ENST00000698632.1:n.3450G>T
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|
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ENST00000698633.1:n.3340G>T
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|
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ENST00000425368.7:c.1844G>T
MANE Select
|
ENSP00000416561.2:p.Cys615Phe
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ENST00000425368.6:c.1844G>T
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ENSP00000416561.2:p.Cys615Phe
|
|
ENST00000456570.5:c.3350G>T
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ENSP00000410815.1:p.Cys1117Phe
|
|
ENST00000467360.1:n.970G>T
|
|
|
ENST00000477310.1:c.2897G>T
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ENSP00000418996.1:p.Cys966Phe
|
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ENST00000482312.1:n.60G>T
|
|
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ENST00000483004.1:c.466G>T
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|
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NM_001710.5:c.1844G>T , LRG_136t1:c.1844G>T
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NP_001701.2:p.Cys615Phe
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|
NM_001710.6:c.1844G>T
MANE Select
|
NP_001701.2:p.Cys615Phe
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