ENST00000446859.7:c.763A>T
MANE Select
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ENSP00000414635.1:p.Thr255Ser
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ENST00000446859.5:c.763A>T
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ENSP00000414635.1:p.Thr255Ser
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ENST00000522080.5:n.740A>T
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|
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ENST00000522329.1:n.12A>T
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|
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ENST00000522526.6:c.667A>T
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ENSP00000429278.2:p.Thr223Ser
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ENST00000522596.6:n.745A>T
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|
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ENST00000522830.5:c.580A>T
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ENSP00000429593.1:p.Thr194Ser
|
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ENST00000524054.5:n.611A>T
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|
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ENST00000524327.5:n.563A>T
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|
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ENST00000528597.1:c.10A>T
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ENSP00000436883.1:p.Thr4Ser
|
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ENST00000602774.1:n.149A>T
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|
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NM_001172779.1:c.763A>T
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NP_001166250.1:p.Thr255Ser
|
|
NM_001172780.1:c.763A>T
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NP_001166251.1:p.Thr255Ser
|
|
NM_153353.4:c.667A>T
|
NP_699184.2:p.Thr223Ser
|
|
XM_005247133.2:c.580A>T
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XP_005247190.1:p.Thr194Ser
|
|
XM_006713508.2:c.709A>T
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XP_006713571.1:p.Thr237Ser
|
|
XM_011512442.1:c.760A>T
|
XP_011510744.1:p.Thr254Ser
|
|
NM_001363888.1:c.580A>T
|
NP_001350817.1:p.Thr194Ser
|
|
XM_006713508.4:c.709A>T
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XP_006713571.1:p.Thr237Ser
|
|
XM_011512442.2:c.760A>T
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XP_011510744.1:p.Thr254Ser
|
|
XM_017005746.1:c.577A>T
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XP_016861235.1:p.Thr193Ser
|
|
NM_001172779.2:c.763A>T
MANE Select
|
NP_001166250.1:p.Thr255Ser
|
|
NM_001172780.2:c.763A>T
|
NP_001166251.1:p.Thr255Ser
|
|
NM_001363888.2:c.580A>T
|
NP_001350817.1:p.Thr194Ser
|
|
NM_001370608.1:c.577A>T
|
NP_001357537.1:p.Thr193Ser
|
|
NM_001370609.1:c.580A>T
|
NP_001357538.1:p.Thr194Ser
|
|
NM_153353.5:c.667A>T
|
NP_699184.2:p.Thr223Ser
|
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