ENST00000314251.8:c.576T=
MANE Select
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ENSP00000323568.3:p.His192=
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ENST00000314251.7:c.576T=
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ENSP00000323568.3:p.His192=
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ENST00000461867.1:c.57T=
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ENSP00000418888.1:p.His19=
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ENST00000469787.1:c.*43T=
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ENSP00000417918.1:n.*43T=
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ENST00000471379.1:n.287T=
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ENST00000497642.5:c.*43T=
|
ENSP00000418456.1:n.*43T=
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NM_000340.1:c.576T=
|
NP_000331.1:p.His192=
|
|
NM_001278658.1:c.219T=
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NP_001265587.1:p.His73=
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NM_001278659.1:c.57T=
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NP_001265588.1:p.His19=
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XM_011513087.1:c.531T=
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XP_011511389.1:p.His177=
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|
XM_011513088.1:c.357T=
|
XP_011511390.1:p.His119=
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|
XM_011513089.1:c.57T=
|
XP_011511391.1:p.His19=
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|
XM_011513087.2:c.531T=
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XP_011511389.1:p.His177=
|
|
XM_024453720.1:c.57T=
|
XP_024309488.1:p.His19=
|
|
NM_000340.2:c.576T=
MANE Select
|
NP_000331.1:p.His192=
|
|
NM_001278658.2:c.219T=
|
NP_001265587.1:p.His73=
|
|
NM_001278659.2:c.57T=
|
NP_001265588.1:p.His19=
|
|