ENST00000366669.9:c.1851G>C
MANE Select
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ENSP00000355629.4:p.Gln617His
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ENST00000366668.7:c.1848G>C
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ENSP00000355628.3:p.Gln616His
|
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ENST00000366669.8:c.1851G>C
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ENSP00000355629.4:p.Gln617His
|
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ENST00000468893.6:c.*1709G>C
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ENSP00000476305.1:n.*1709G>C
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ENST00000478710.1:n.110G>C
|
|
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ENST00000490900.1:n.630G>C
|
|
|
ENST00000534989.1:c.1674G>C
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ENSP00000440349.1:p.Gln558His
|
|
NM_001145036.1:c.1848G>C
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NP_001138508.1:p.Gln616His
|
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NM_007357.2:c.1851G>C
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NP_031383.1:p.Gln617His
|
|
NM_007357.3:c.1851G>C
MANE Select
|
NP_031383.1:p.Gln617His
|
|
NM_001145036.2:c.1848G>C
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NP_001138508.1:p.Gln616His
|
|