ENST00000267845.8:c.1700C>A
MANE Select
|
ENSP00000267845.3:p.Ser567Tyr
|
|
ENST00000267845.7:c.1700C>A
|
ENSP00000267845.3:p.Ser567Tyr
|
|
ENST00000543581.5:c.1601C>A
|
ENSP00000440252.1:p.Ser534Tyr
|
|
ENST00000559816.1:n.1444C>A
|
|
|
NM_001306146.1:c.1601C>A
|
NP_001293075.1:p.Ser534Tyr
|
|
NM_002112.3:c.1700C>A
|
NP_002103.2:p.Ser567Tyr
|
|
XM_011521479.1:c.1463C>A
|
XP_011519781.1:p.Ser488Tyr
|
|
XM_011521480.1:c.1268C>A
|
XP_011519782.1:p.Ser423Tyr
|
|
XM_017022094.1:c.1805C>A
|
XP_016877583.1:p.Ser602Tyr
|
|
XM_017022095.1:c.1706C>A
|
XP_016877584.1:p.Ser569Tyr
|
|
XM_017022096.1:c.1577C>A
|
XP_016877585.1:p.Ser526Tyr
|
|
XM_017022097.1:c.1568C>A
|
XP_016877586.1:p.Ser523Tyr
|
|
XM_017022098.1:c.1373C>A
|
XP_016877587.1:p.Ser458Tyr
|
|
NM_002112.4:c.1700C>A
MANE Select
|
NP_002103.2:p.Ser567Tyr
|
|
NM_001306146.2:c.1601C>A
|
NP_001293075.1:p.Ser534Tyr
|
|