ENST00000370263.9:c.555C>G
MANE Select
|
ENSP00000359285.4:p.Asp185Glu
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ENST00000370263.8:c.555C>G
|
ENSP00000359285.4:p.Asp185Glu
|
|
ENST00000463705.5:n.1203C>G
|
|
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ENST00000467563.3:n.625C>G
|
|
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ENST00000498043.6:c.579C>G
|
|
|
ENST00000615287.4:c.342C>G
|
ENSP00000483388.1:p.Asp114Glu
|
|
ENST00000627000.1:c.*244C>G
|
ENSP00000486914.1:n.*244C>G
|
|
ENST00000630240.1:n.276C>G
|
|
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NM_000744.6:c.555C>G
|
NP_000735.1:p.Asp185Glu
|
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NM_001256573.1:c.27C>G
|
NP_001243502.1:p.Asp9Glu
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NR_046317.1:n.811C>G
|
|
|
XM_011528524.1:c.342C>G
|
XP_011526826.1:p.Asp114Glu
|
|
XM_017027625.2:c.27C>G
|
XP_016883114.1:p.Asp9Glu
|
|
XM_024451822.1:c.27C>G
|
XP_024307590.1:p.Asp9Glu
|
|
NM_001256573.2:c.27C>G
|
NP_001243502.1:p.Asp9Glu
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NR_046317.2:n.764C>G
|
|
|
NM_000744.7:c.555C>G
MANE Select
|
NP_000735.1:p.Asp185Glu
|
|