ENST00000264595.7:c.487T>C
MANE Select
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ENSP00000264595.2:p.Cys163Arg
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ENST00000264595.6:c.487T>C
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ENSP00000264595.2:p.Cys163Arg
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ENST00000502310.5:c.142T>C
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ENSP00000423798.1:p.Cys48Arg
|
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ENST00000506853.5:n.521T>C
|
|
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ENST00000510635.1:c.183T>C
|
|
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ENST00000510955.5:n.408T>C
|
|
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NM_000027.3:c.487T>C
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NP_000018.2:p.Cys163Arg
|
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NM_001171988.1:c.487T>C
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NP_001165459.1:p.Cys163Arg
|
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NR_033655.1:n.615T>C
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XM_006714123.2:c.487T>C
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XP_006714186.1:p.Cys163Arg
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XR_001741155.2:n.581T>C
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|
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NM_000027.4:c.487T>C
MANE Select
|
NP_000018.2:p.Cys163Arg
|
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NM_001171988.2:c.487T>C
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NP_001165459.1:p.Cys163Arg
|
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NR_033655.2:n.549T>C
|
|
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