ENST00000263121.12:c.938C>T
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ENSP00000263121.8:p.Ala313Val
|
|
ENST00000344921.11:c.1103C>T
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ENSP00000340883.6:p.Ala368Val
|
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ENST00000407422.8:c.1049C>T
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ENSP00000383984.3:p.Ala350Val
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ENST00000644036.2:c.1076C>T
MANE Select
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ENSP00000494049.2:p.Ala359Val
|
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ENST00000644462.1:c.1794C>T
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ENSP00000494283.1:n.1794C>T
|
|
ENST00000645799.1:n.2398C>T
|
|
|
ENST00000646723.1:n.3422C>T
|
|
|
ENST00000647057.1:c.*570C>T
|
ENSP00000494757.1:n.*570C>T
|
|
ENST00000263121.11:c.1076C>T
|
ENSP00000263121.7:p.Ala359Val
|
|
ENST00000344921.10:c.1103C>T
|
ENSP00000340883.6:p.Ala368Val
|
|
ENST00000407082.3:c.938C>T
|
ENSP00000385226.3:p.Ala313Val
|
|
ENST00000407422.7:c.1049C>T
|
ENSP00000383984.3:p.Ala350Val
|
|
NM_001007468.1:c.1049C>T
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NP_001007469.1:p.Ala350Val
|
|
NM_003073.3:c.1076C>T , LRG_520t1:c.1076C>T
|
NP_003064.2:p.Ala359Val
|
|
XM_011530345.1:c.1130C>T
|
XP_011528647.1:p.Ala377Val
|
|
XM_011530346.1:c.1103C>T
|
XP_011528648.1:p.Ala368Val
|
|
NM_001007468.2:c.1049C>T
|
NP_001007469.1:p.Ala350Val
|
|
NM_001317946.1:c.1103C>T
|
NP_001304875.1:p.Ala368Val
|
|
NM_001362877.1:c.1130C>T
|
NP_001349806.1:p.Ala377Val
|
|
NM_003073.4:c.1076C>T
|
NP_003064.2:p.Ala359Val
|
|
NM_001007468.3:c.1049C>T
|
NP_001007469.1:p.Ala350Val
|
|
NM_001317946.2:c.1103C>T
|
NP_001304875.1:p.Ala368Val
|
|
NM_001362877.2:c.1130C>T
|
NP_001349806.1:p.Ala377Val
|
|
NM_003073.5:c.1076C>T
MANE Select
|
NP_003064.2:p.Ala359Val
|
|