ENST00000375559.8:c.1322A>C
MANE Select
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ENSP00000364709.3:p.Glu441Ala
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ENST00000375551.7:c.*313A>C
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ENSP00000364701.3:n.*313A>C
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ENST00000375559.7:c.1322A>C
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ENSP00000364709.3:p.Glu441Ala
|
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ENST00000409306.5:c.*313A>C
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ENSP00000387092.1:n.*313A>C
|
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NM_000504.3:c.1322A>C , LRG_548t1:c.1322A>C
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NP_000495.1:p.Glu441Ala
|
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NM_001312674.1:c.1190A>C
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NP_001299603.1:p.Glu397Ala
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NM_001312675.1:c.*313A>C
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NP_001299604.1:n.*313A>C
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NM_000504.4:c.1322A>C
MANE Select
|
NP_000495.1:p.Glu441Ala
|
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NM_001312674.2:c.1190A>C
|
NP_001299603.1:p.Glu397Ala
|
|
NM_001312675.2:c.*313A>C
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NP_001299604.1:n.*313A>C
|
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