ENST00000370263.9:c.818A>T
MANE Select
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ENSP00000359285.4:p.Glu273Val
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ENST00000370263.8:c.818A>T
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ENSP00000359285.4:p.Glu273Val
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ENST00000463705.5:n.1466A>T
|
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ENST00000467563.3:n.888A>T
|
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ENST00000498043.6:c.842A>T
|
|
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ENST00000615287.4:c.605A>T
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ENSP00000483388.1:p.Glu202Val
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ENST00000627000.1:c.*507A>T
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ENSP00000486914.1:n.*507A>T
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ENST00000630240.1:n.539A>T
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NM_000744.6:c.818A>T
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NP_000735.1:p.Glu273Val
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NM_001256573.1:c.290A>T
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NP_001243502.1:p.Glu97Val
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NR_046317.1:n.1074A>T
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XM_011528524.1:c.605A>T
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XP_011526826.1:p.Glu202Val
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XM_017027625.2:c.290A>T
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XP_016883114.1:p.Glu97Val
|
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XM_024451822.1:c.290A>T
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XP_024307590.1:p.Glu97Val
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NM_001256573.2:c.290A>T
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NP_001243502.1:p.Glu97Val
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NR_046317.2:n.1027A>T
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NM_000744.7:c.818A>T
MANE Select
|
NP_000735.1:p.Glu273Val
|
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