ENST00000356392.9:c.1129C=
MANE Select
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ENSP00000348757.3:p.Arg377=
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|
ENST00000356392.8:c.1129C=
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ENSP00000348757.3:p.Arg377=
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|
ENST00000586836.5:c.556C=
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ENSP00000467429.1:p.Arg186=
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|
ENST00000591179.5:c.949C=
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ENSP00000466800.1:p.Arg317=
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|
ENST00000591345.5:c.*1048C=
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ENSP00000467313.1:n.*1048C=
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|
NM_001302453.1:c.967C=
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NP_001289382.1:p.Arg323=
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|
NM_001302454.1:c.949C=
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NP_001289383.1:p.Arg317=
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|
NM_145045.4:c.1129C=
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NP_659482.3:p.Arg377=
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|
XM_017026241.1:c.*23C=
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XP_016881730.1:n.*23C=
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|
NM_145045.5:c.1129C=
MANE Select
|
NP_659482.3:p.Arg377=
|
|
NM_001302454.2:c.949C=
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NP_001289383.1:p.Arg317=
|
|