ENST00000433363.7:c.843T=
MANE Select
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ENSP00000406220.2:p.Phe281=
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ENST00000293800.10:c.792T=
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ENSP00000293800.6:p.Phe264=
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|
ENST00000381074.8:c.714T=
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ENSP00000370464.4:p.Phe238=
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|
ENST00000433363.6:c.843T=
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ENSP00000406220.2:p.Phe281=
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ENST00000572094.1:c.*593T=
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ENSP00000461495.1:n.*593T=
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|
ENST00000573648.5:c.843T=
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ENSP00000459372.1:p.Phe281=
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|
ENST00000574824.5:n.1976T=
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|
|
NM_001143838.2:c.843T=
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NP_001137310.1:p.Phe281=
|
|
NM_001284509.1:c.792T=
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NP_001271438.1:p.Phe264=
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|
NM_001284510.1:c.714T=
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NP_001271439.1:p.Phe238=
|
|
NM_177550.4:c.843T= , LRG_1020t1:c.843T=
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NP_808218.1:p.Phe281=
|
|
XM_006721504.2:c.732T=
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XP_006721567.1:p.Phe244=
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|
XM_011523795.1:c.843T=
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XP_011522097.1:p.Phe281=
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|
XM_011523795.3:c.843T=
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XP_011522097.1:p.Phe281=
|
|
NM_001143838.3:c.843T=
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NP_001137310.1:p.Phe281=
|
|
NM_001284509.2:c.792T=
|
NP_001271438.1:p.Phe264=
|
|
NM_001284510.2:c.714T=
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NP_001271439.1:p.Phe238=
|
|
NM_177550.5:c.843T=
MANE Select
|
NP_808218.1:p.Phe281=
|
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