ENST00000355832.10:c.3702A>T
MANE Select
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ENSP00000348089.5:p.Gln1234His
|
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ENST00000679552.1:n.773A>T
|
|
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ENST00000679871.1:n.848A>T
|
|
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ENST00000679974.1:n.751A>T
|
|
|
ENST00000681632.1:n.5105A>T
|
|
|
ENST00000681659.1:c.3543A>T
|
ENSP00000505631.1:p.Gln1181His
|
|
ENST00000355832.9:c.3702A>T
|
ENSP00000348089.5:p.Gln1234His
|
|
ENST00000465653.1:n.24A>T
|
|
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ENST00000623073.3:c.*1998A>T
|
ENSP00000485650.1:n.*1998A>T
|
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ENST00000623115.3:c.1812A>T
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ENSP00000485321.1:p.Gln604His
|
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ENST00000624341.3:c.1534A>T
|
|
|
NM_000124.3:c.3702A>T
|
NP_000115.1:p.Gln1234His
|
|
XR_945953.1:n.243-1307T>A
|
|
|
NM_001346440.1:c.3702A>T
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NP_001333369.1:p.Gln1234His
|
|
NM_000124.4:c.3702A>T
MANE Select
|
NP_000115.1:p.Gln1234His
|
|
NM_001346440.2:c.3702A>T
|
NP_001333369.1:p.Gln1234His
|
|