ENST00000267845.8:c.1761C>A
MANE Select
|
ENSP00000267845.3:p.Cys587Ter
|
|
ENST00000267845.7:c.1761C>A
|
ENSP00000267845.3:p.Cys587Ter
|
|
ENST00000543581.5:c.1662C>A
|
ENSP00000440252.1:p.Cys554Ter
|
|
ENST00000559816.1:n.1505C>A
|
|
|
NM_001306146.1:c.1662C>A
|
NP_001293075.1:p.Cys554Ter
|
|
NM_002112.3:c.1761C>A
|
NP_002103.2:p.Cys587Ter
|
|
XM_011521479.1:c.1524C>A
|
XP_011519781.1:p.Cys508Ter
|
|
XM_011521480.1:c.1329C>A
|
XP_011519782.1:p.Cys443Ter
|
|
XM_017022094.1:c.1866C>A
|
XP_016877583.1:p.Cys622Ter
|
|
XM_017022095.1:c.1767C>A
|
XP_016877584.1:p.Cys589Ter
|
|
XM_017022096.1:c.1638C>A
|
XP_016877585.1:p.Cys546Ter
|
|
XM_017022097.1:c.1629C>A
|
XP_016877586.1:p.Cys543Ter
|
|
XM_017022098.1:c.1434C>A
|
XP_016877587.1:p.Cys478Ter
|
|
NM_002112.4:c.1761C>A
MANE Select
|
NP_002103.2:p.Cys587Ter
|
|
NM_001306146.2:c.1662C>A
|
NP_001293075.1:p.Cys554Ter
|
|