ENST00000649865.1:c.1461C>G
|
ENSP00000496919.1:p.Ser487=
|
|
ENST00000650285.1:c.1461C>G
MANE Select
|
ENSP00000497069.1:p.Ser487=
|
|
ENST00000268035.10:c.1461C>G
|
ENSP00000268035.6:p.Ser487=
|
|
ENST00000558762.5:c.1461C>G
|
ENSP00000453007.1:p.Ser487=
|
|
ENST00000558898.1:c.552C>G
|
ENSP00000454115.1:p.Ser184=
|
|
ENST00000559582.1:n.368C>G
|
|
|
ENST00000559925.5:n.1461C>G
|
|
|
NM_000875.4:c.1461C>G
|
NP_000866.1:p.Ser487=
|
|
NM_001291858.1:c.1461C>G
|
NP_001278787.1:p.Ser487=
|
|
XM_011521513.1:c.1524C>G
|
XP_011519815.1:p.Ser508=
|
|
XM_011521514.1:c.1524C>G
|
XP_011519816.1:p.Ser508=
|
|
XM_011521515.1:c.1524C>G
|
XP_011519817.1:p.Ser508=
|
|
XM_011521516.1:c.552C>G
|
XP_011519818.1:p.Ser184=
|
|
XM_011521517.1:c.126C>G
|
XP_011519819.1:p.Ser42=
|
|
XM_011521516.2:c.552C>G
|
XP_011519818.1:p.Ser184=
|
|
XM_011521517.2:c.126C>G
|
XP_011519819.1:p.Ser42=
|
|
XM_017022136.1:c.1536C>G
|
XP_016877625.1:p.Ser512=
|
|
XM_017022137.1:c.1536C>G
|
XP_016877626.1:p.Ser512=
|
|
XM_017022138.1:c.1536C>G
|
XP_016877627.1:p.Ser512=
|
|
XM_017022139.1:c.1098C>G
|
XP_016877628.1:p.Ser366=
|
|
XM_024449913.1:c.552C>G
|
XP_024305681.1:p.Ser184=
|
|
NM_000875.5:c.1461C>G
MANE Select
|
NP_000866.1:p.Ser487=
|
|
NM_001291858.2:c.1461C>G
|
NP_001278787.1:p.Ser487=
|
|