ENST00000614565.5:c.1841A>C
MANE Select
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ENSP00000484928.1:p.Glu614Ala
|
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ENST00000543233.2:c.1619A>C
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ENSP00000443301.1:p.Glu540Ala
|
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ENST00000611855.4:c.1559A>C
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ENSP00000480844.1:p.Glu520Ala
|
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ENST00000614565.4:c.1841A>C
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ENSP00000484928.1:p.Glu614Ala
|
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NM_001252338.2:c.1730A>C
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NP_001239267.1:p.Glu577Ala
|
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NM_001252339.2:c.1619A>C
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NP_001239268.1:p.Glu540Ala
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NM_001794.4:c.1841A>C
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NP_001785.2:p.Glu614Ala
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NM_001794.5:c.1841A>C
MANE Select
|
NP_001785.2:p.Glu614Ala
|
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NM_001252339.3:c.1619A>C
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NP_001239268.1:p.Glu540Ala
|
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