ENST00000267845.8:c.1700C>G
MANE Select
|
ENSP00000267845.3:p.Ser567Cys
|
|
ENST00000267845.7:c.1700C>G
|
ENSP00000267845.3:p.Ser567Cys
|
|
ENST00000543581.5:c.1601C>G
|
ENSP00000440252.1:p.Ser534Cys
|
|
ENST00000559816.1:n.1444C>G
|
|
|
NM_001306146.1:c.1601C>G
|
NP_001293075.1:p.Ser534Cys
|
|
NM_002112.3:c.1700C>G
|
NP_002103.2:p.Ser567Cys
|
|
XM_011521479.1:c.1463C>G
|
XP_011519781.1:p.Ser488Cys
|
|
XM_011521480.1:c.1268C>G
|
XP_011519782.1:p.Ser423Cys
|
|
XM_017022094.1:c.1805C>G
|
XP_016877583.1:p.Ser602Cys
|
|
XM_017022095.1:c.1706C>G
|
XP_016877584.1:p.Ser569Cys
|
|
XM_017022096.1:c.1577C>G
|
XP_016877585.1:p.Ser526Cys
|
|
XM_017022097.1:c.1568C>G
|
XP_016877586.1:p.Ser523Cys
|
|
XM_017022098.1:c.1373C>G
|
XP_016877587.1:p.Ser458Cys
|
|
NM_002112.4:c.1700C>G
MANE Select
|
NP_002103.2:p.Ser567Cys
|
|
NM_001306146.2:c.1601C>G
|
NP_001293075.1:p.Ser534Cys
|
|