ENST00000267845.8:c.1760G>C
MANE Select
|
ENSP00000267845.3:p.Cys587Ser
|
|
ENST00000267845.7:c.1760G>C
|
ENSP00000267845.3:p.Cys587Ser
|
|
ENST00000543581.5:c.1661G>C
|
ENSP00000440252.1:p.Cys554Ser
|
|
ENST00000559816.1:n.1504G>C
|
|
|
NM_001306146.1:c.1661G>C
|
NP_001293075.1:p.Cys554Ser
|
|
NM_002112.3:c.1760G>C
|
NP_002103.2:p.Cys587Ser
|
|
XM_011521479.1:c.1523G>C
|
XP_011519781.1:p.Cys508Ser
|
|
XM_011521480.1:c.1328G>C
|
XP_011519782.1:p.Cys443Ser
|
|
XM_017022094.1:c.1865G>C
|
XP_016877583.1:p.Cys622Ser
|
|
XM_017022095.1:c.1766G>C
|
XP_016877584.1:p.Cys589Ser
|
|
XM_017022096.1:c.1637G>C
|
XP_016877585.1:p.Cys546Ser
|
|
XM_017022097.1:c.1628G>C
|
XP_016877586.1:p.Cys543Ser
|
|
XM_017022098.1:c.1433G>C
|
XP_016877587.1:p.Cys478Ser
|
|
NM_002112.4:c.1760G>C
MANE Select
|
NP_002103.2:p.Cys587Ser
|
|
NM_001306146.2:c.1661G>C
|
NP_001293075.1:p.Cys554Ser
|
|