ENST00000682297.1:n.273T>G
|
|
|
ENST00000682868.1:n.6891T>G
|
|
|
ENST00000682871.1:c.4942T>G
|
ENSP00000507805.1:p.Cys1648Gly
|
|
ENST00000684506.1:c.*3474T>G
|
ENSP00000507728.1:n.*3474T>G
|
|
ENST00000684607.1:c.4942T>G
|
ENSP00000508224.1:p.Cys1648Gly
|
|
ENST00000295956.9:c.4849T>G
MANE Select
|
ENSP00000295956.5:p.Cys1617Gly
|
|
ENST00000295956.8:c.4849T>G
|
ENSP00000295956.4:p.Cys1617Gly
|
|
ENST00000358537.7:c.4849T>G
|
ENSP00000351339.3:p.Cys1617Gly
|
|
ENST00000429972.6:c.4849T>G
|
ENSP00000415599.2:p.Cys1617Gly
|
|
ENST00000481470.5:n.1189T>G
|
|
|
ENST00000490882.5:c.4942T>G
|
ENSP00000420213.1:p.Cys1648Gly
|
|
ENST00000493452.5:c.4342T>G
|
ENSP00000418510.1:p.Cys1448Gly
|
|
NM_001164317.1:c.4942T>G
|
NP_001157789.1:p.Cys1648Gly
|
|
NM_001164318.1:c.4849T>G
|
NP_001157790.1:p.Cys1617Gly
|
|
NM_001164319.1:c.4849T>G
|
NP_001157791.1:p.Cys1617Gly
|
|
NM_001457.3:c.4849T>G
|
NP_001448.2:p.Cys1617Gly
|
|
XM_005264977.1:c.4942T>G
|
XP_005265034.1:p.Cys1648Gly
|
|
XM_005264978.1:c.4942T>G
|
XP_005265035.1:p.Cys1648Gly
|
|
XM_005264981.1:c.4942T>G
|
XP_005265038.1:p.Cys1648Gly
|
|
XR_940396.1:n.5087T>G
|
|
|
XM_005264978.2:c.4942T>G
|
XP_005265035.1:p.Cys1648Gly
|
|
XR_001740065.1:n.5087T>G
|
|
|
XR_940396.2:n.5087T>G
|
|
|
NM_001164317.2:c.4942T>G
|
NP_001157789.1:p.Cys1648Gly
|
|
NM_001164318.2:c.4849T>G
|
NP_001157790.1:p.Cys1617Gly
|
|
NM_001164319.2:c.4849T>G
|
NP_001157791.1:p.Cys1617Gly
|
|
NM_001457.4:c.4849T>G
MANE Select
|
NP_001448.2:p.Cys1617Gly
|
|