ENST00000370263.9:c.1712T>G
MANE Select
|
ENSP00000359285.4:p.Val571Gly
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ENST00000370263.8:c.1712T>G
|
ENSP00000359285.4:p.Val571Gly
|
|
ENST00000463705.5:n.2360T>G
|
|
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ENST00000467563.3:n.1782T>G
|
|
|
ENST00000498043.6:c.1736T>G
|
|
|
ENST00000615287.4:c.1499T>G
|
ENSP00000483388.1:p.Val500Gly
|
|
ENST00000627000.1:c.*1401T>G
|
ENSP00000486914.1:n.*1401T>G
|
|
ENST00000630240.1:n.1433T>G
|
|
|
NM_000744.6:c.1712T>G
|
NP_000735.1:p.Val571Gly
|
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NM_001256573.1:c.1184T>G
|
NP_001243502.1:p.Val395Gly
|
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NR_046317.1:n.1968T>G
|
|
|
XM_011528524.1:c.1499T>G
|
XP_011526826.1:p.Val500Gly
|
|
XM_017027625.2:c.1184T>G
|
XP_016883114.1:p.Val395Gly
|
|
XM_024451822.1:c.1184T>G
|
XP_024307590.1:p.Val395Gly
|
|
NM_001256573.2:c.1184T>G
|
NP_001243502.1:p.Val395Gly
|
|
NR_046317.2:n.1921T>G
|
|
|
NM_000744.7:c.1712T>G
MANE Select
|
NP_000735.1:p.Val571Gly
|
|