ENST00000355832.10:c.3492A>T
MANE Select
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ENSP00000348089.5:p.Gln1164His
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ENST00000679552.1:n.563A>T
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|
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ENST00000679871.1:n.638A>T
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|
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ENST00000679974.1:n.541A>T
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|
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ENST00000681632.1:n.4895A>T
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|
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ENST00000681659.1:c.3333A>T
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ENSP00000505631.1:p.Gln1111His
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ENST00000355832.9:c.3492A>T
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ENSP00000348089.5:p.Gln1164His
|
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ENST00000623073.3:c.*1788A>T
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ENSP00000485650.1:n.*1788A>T
|
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ENST00000623115.3:c.1602A>T
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ENSP00000485321.1:p.Gln534His
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ENST00000624341.3:c.1324A>T
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NM_000124.3:c.3492A>T
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NP_000115.1:p.Gln1164His
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XR_945953.1:n.243-1097T>A
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|
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NM_001346440.1:c.3492A>T
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NP_001333369.1:p.Gln1164His
|
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NM_000124.4:c.3492A>T
MANE Select
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NP_000115.1:p.Gln1164His
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NM_001346440.2:c.3492A>T
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NP_001333369.1:p.Gln1164His
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