ENST00000350051.8:c.415G>T
MANE Select
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ENSP00000324180.4:p.Ala139Ser
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ENST00000301633.8:c.484G>T
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ENSP00000301633.3:p.Ala162Ser
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ENST00000350051.7:c.415G>T
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ENSP00000324180.4:p.Ala139Ser
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ENST00000374948.6:c.297G>T
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ENSP00000364086.1:p.Trp99Cys
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ENST00000589892.1:n.431G>T
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ENST00000590925.6:c.*217G>T
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ENSP00000467336.1:n.*217G>T
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NM_001012270.1:c.297G>T
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NP_001012270.1:p.Trp99Cys
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NM_001012271.1:c.484G>T
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NP_001012271.1:p.Ala162Ser
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NM_001168.2:c.415G>T
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NP_001159.2:p.Ala139Ser
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XR_243654.3:n.617G>T
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XR_934452.1:n.686G>T
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|
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XR_243654.5:n.617G>T
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|
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XR_934452.3:n.686G>T
|
|
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NM_001168.3:c.415G>T
MANE Select
|
NP_001159.2:p.Ala139Ser
|
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NM_001012270.2:c.297G>T
|
NP_001012270.1:p.Trp99Cys
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NM_001012271.2:c.484G>T
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NP_001012271.1:p.Ala162Ser
|
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