ENST00000695651.1:n.849G=
|
|
|
ENST00000695652.1:c.2378G=
|
ENSP00000512083.1:p.Arg793=
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|
ENST00000695653.1:c.410G=
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ENSP00000512084.1:p.Arg137=
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ENST00000695654.1:c.1625G=
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ENSP00000512085.1:p.Arg542=
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ENST00000695655.1:c.1442G=
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ENSP00000512086.1:n.1442G=
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|
ENST00000695692.1:n.1865G=
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|
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ENST00000245907.11:c.2501G=
MANE Select
|
ENSP00000245907.4:p.Arg834=
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ENST00000245907.10:c.2501G=
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ENSP00000245907.4:p.Arg834=
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ENST00000602053.1:n.549G=
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NM_000064.3:c.2501G=
|
NP_000055.2:p.Arg834=
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|
NM_000064.4:c.2501G=
MANE Select
|
NP_000055.2:p.Arg834=
|
|