ENST00000398603.6:c.347C>T
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ENSP00000381604.1:p.Ala116Val
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|
ENST00000398606.10:c.455C>T
MANE Select
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ENSP00000381607.3:p.Ala152Val
|
|
ENST00000646888.1:c.*171C>T
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ENSP00000494477.1:n.*171C>T
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|
ENST00000398603.5:c.347C>T
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ENSP00000381604.1:p.Ala116Val
|
|
ENST00000398606.7:c.455C>T
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ENSP00000381607.3:p.Ala152Val
|
|
ENST00000467591.1:n.566C>T
|
|
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ENST00000494593.1:n.1427C>T
|
|
|
ENST00000495996.1:c.181C>T
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ENSP00000484686.1:p.Leu61=
|
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ENST00000498765.5:c.518C>T
|
|
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NM_000852.3:c.455C>T , LRG_723t1:c.455C>T
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NP_000843.1:p.Ala152Val
|
|
NM_000852.4:c.455C>T
MANE Select
|
NP_000843.1:p.Ala152Val
|
|