ENST00000267845.8:c.1760G>T
MANE Select
|
ENSP00000267845.3:p.Cys587Phe
|
|
ENST00000267845.7:c.1760G>T
|
ENSP00000267845.3:p.Cys587Phe
|
|
ENST00000543581.5:c.1661G>T
|
ENSP00000440252.1:p.Cys554Phe
|
|
ENST00000559816.1:n.1504G>T
|
|
|
NM_001306146.1:c.1661G>T
|
NP_001293075.1:p.Cys554Phe
|
|
NM_002112.3:c.1760G>T
|
NP_002103.2:p.Cys587Phe
|
|
XM_011521479.1:c.1523G>T
|
XP_011519781.1:p.Cys508Phe
|
|
XM_011521480.1:c.1328G>T
|
XP_011519782.1:p.Cys443Phe
|
|
XM_017022094.1:c.1865G>T
|
XP_016877583.1:p.Cys622Phe
|
|
XM_017022095.1:c.1766G>T
|
XP_016877584.1:p.Cys589Phe
|
|
XM_017022096.1:c.1637G>T
|
XP_016877585.1:p.Cys546Phe
|
|
XM_017022097.1:c.1628G>T
|
XP_016877586.1:p.Cys543Phe
|
|
XM_017022098.1:c.1433G>T
|
XP_016877587.1:p.Cys478Phe
|
|
NM_002112.4:c.1760G>T
MANE Select
|
NP_002103.2:p.Cys587Phe
|
|
NM_001306146.2:c.1661G>T
|
NP_001293075.1:p.Cys554Phe
|
|