ENST00000366669.9:c.1884A>G
MANE Select
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ENSP00000355629.4:p.Gln628=
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ENST00000366668.7:c.1881A>G
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ENSP00000355628.3:p.Gln627=
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ENST00000366669.8:c.1884A>G
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ENSP00000355629.4:p.Gln628=
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ENST00000468893.6:c.*1742A>G
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ENSP00000476305.1:n.*1742A>G
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ENST00000478710.1:n.143A>G
|
|
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ENST00000490900.1:n.663A>G
|
|
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ENST00000534989.1:c.1707A>G
|
ENSP00000440349.1:p.Gln569=
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|
NM_001145036.1:c.1881A>G
|
NP_001138508.1:p.Gln627=
|
|
NM_007357.2:c.1884A>G
|
NP_031383.1:p.Gln628=
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|
NM_007357.3:c.1884A>G
MANE Select
|
NP_031383.1:p.Gln628=
|
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NM_001145036.2:c.1881A>G
|
NP_001138508.1:p.Gln627=
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