ENST00000337523.10:c.1177C>G
MANE Select
|
ENSP00000337759.5:p.Pro393Ala
|
|
ENST00000337523.9:c.1177C>G
|
ENSP00000337759.5:p.Pro393Ala
|
|
ENST00000375349.7:c.1177C>G
|
ENSP00000364498.3:p.Pro393Ala
|
|
ENST00000375356.7:c.1177C>G
|
ENSP00000364505.3:p.Pro393Ala
|
|
ENST00000473976.1:n.1949C>G
|
|
|
ENST00000477826.5:n.2012C>G
|
|
|
ENST00000478221.5:n.1058C>G
|
|
|
ENST00000485557.5:n.1797C>G
|
|
|
ENST00000491327.5:n.1314C>G
|
|
|
ENST00000495340.5:c.510C>G
|
|
|
ENST00000498357.1:n.1621C>G
|
|
|
NM_005510.3:c.1177C>G
|
NP_005501.2:p.Pro393Ala
|
|
XM_006715005.2:c.1177C>G
|
XP_006715068.1:p.Pro393Ala
|
|
XM_006715007.2:c.625C>G
|
XP_006715070.1:p.Pro209Ala
|
|
XR_926081.1:n.1650C>G
|
|
|
XR_926082.1:n.1677C>G
|
|
|
XM_006715005.3:c.1177C>G
|
XP_006715068.1:p.Pro393Ala
|
|
XM_017010329.1:c.625C>G
|
XP_016865818.1:p.Pro209Ala
|
|
XR_002956262.1:n.1409C>G
|
|
|
XR_002956263.1:n.1575C>G
|
|
|
XR_002956264.1:n.1475C>G
|
|
|
XR_926082.2:n.1417C>G
|
|
|
NM_005510.4:c.1177C>G
MANE Select
|
NP_005501.2:p.Pro393Ala
|
|
NM_001371205.1:c.625C>G
|
NP_001358134.1:p.Pro209Ala
|
|
NM_001371206.1:c.625C>G
|
NP_001358135.1:p.Pro209Ala
|
|