ENST00000355943.8:c.1099G>C
MANE Select
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ENSP00000348211.3:p.Glu367Gln
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ENST00000355943.7:c.1099G>C
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ENSP00000348211.3:p.Glu367Gln
|
|
ENST00000447245.6:c.856G>C
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ENSP00000399717.2:p.Glu286Gln
|
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ENST00000502462.6:n.1415G>C
|
|
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ENST00000504098.1:c.661G>C
|
ENSP00000425708.1:p.Glu221Gln
|
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ENST00000509432.1:c.460G>C
|
ENSP00000426604.1:p.Glu154Gln
|
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ENST00000513706.2:n.2699G>C
|
|
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ENST00000513807.5:c.613G>C
|
ENSP00000421134.1:p.Glu205Gln
|
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NM_001303249.1:c.856G>C
|
NP_001290178.1:p.Glu286Gln
|
|
NM_001303250.1:c.826G>C
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NP_001290179.1:p.Glu276Gln
|
|
NM_138773.2:c.1099G>C
|
NP_620128.1:p.Glu367Gln
|
|
NM_001303249.2:c.856G>C
|
NP_001290178.1:p.Glu286Gln
|
|
NM_001303250.2:c.826G>C
|
NP_001290179.1:p.Glu276Gln
|
|
NM_138773.3:c.1099G>C
|
NP_620128.1:p.Glu367Gln
|
|
NR_138151.1:n.1373G>C
|
|
|
NM_138773.4:c.1099G>C
MANE Select
|
NP_620128.1:p.Glu367Gln
|
|
NM_001303249.3:c.856G>C
|
NP_001290178.1:p.Glu286Gln
|
|
NM_001303250.3:c.826G>C
|
NP_001290179.1:p.Glu276Gln
|
|
NR_138151.2:n.1338G>C
|
|
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