NM_000342.4:c.2279G=
MANE Select
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NP_000333.1:p.Arg760=
|
ENST00000262418.12:c.2279G=
MANE Select
|
ENSP00000262418.6:p.Arg760=
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NM_000342.3:c.2279G=
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NP_000333.1:p.Arg760=
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ENST00000262418.10:c.2279G=
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ENSP00000262418.6:p.Arg760=
|
ENST00000399246.3:c.1181G=
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ENSP00000382190.3:p.Arg394=
|
XM_005257593.3:c.2084G=
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XP_005257650.1:p.Arg695=
|
XM_005257593.5:c.2084G=
|
XP_005257650.1:p.Arg695=
|
XM_011525129.1:c.2189G=
|
XP_011523431.1:p.Arg730=
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XM_011525129.2:c.2189G=
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XP_011523431.1:p.Arg730=
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XM_011525130.1:c.2279G=
|
XP_011523432.1:p.Arg760=
|