ENST00000452035.7:n.2127C>G
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|
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ENST00000483004.2:c.1519C>G
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ENSP00000419887.2:p.Leu507Val
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ENST00000698628.1:c.1624+326C>G
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ENSP00000513848.1:n.1624+326C>G
|
|
ENST00000698629.1:n.1912C>G
|
|
|
ENST00000698630.1:n.2451C>G
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|
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ENST00000698631.1:n.2452C>G
|
|
|
ENST00000698632.1:n.3246C>G
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|
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ENST00000698633.1:n.3136C>G
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|
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ENST00000698636.1:n.1957C>G
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|
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ENST00000425368.7:c.1735C>G
MANE Select
|
ENSP00000416561.2:p.Leu579Val
|
|
ENST00000425368.6:c.1735C>G
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ENSP00000416561.2:p.Leu579Val
|
|
ENST00000456570.5:c.3241C>G
|
ENSP00000410815.1:p.Leu1081Val
|
|
ENST00000467360.1:n.861C>G
|
|
|
ENST00000477310.1:c.2788C>G
|
ENSP00000418996.1:p.Leu930Val
|
|
ENST00000483004.1:c.357C>G
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|
|
NM_001710.5:c.1735C>G , LRG_136t1:c.1735C>G
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NP_001701.2:p.Leu579Val
|
|
NM_001710.6:c.1735C>G
MANE Select
|
NP_001701.2:p.Leu579Val
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