ENST00000267845.8:c.1709T>G
MANE Select
|
ENSP00000267845.3:p.Phe570Cys
|
|
ENST00000267845.7:c.1709T>G
|
ENSP00000267845.3:p.Phe570Cys
|
|
ENST00000543581.5:c.1610T>G
|
ENSP00000440252.1:p.Phe537Cys
|
|
ENST00000559816.1:n.1453T>G
|
|
|
NM_001306146.1:c.1610T>G
|
NP_001293075.1:p.Phe537Cys
|
|
NM_002112.3:c.1709T>G
|
NP_002103.2:p.Phe570Cys
|
|
XM_011521479.1:c.1472T>G
|
XP_011519781.1:p.Phe491Cys
|
|
XM_011521480.1:c.1277T>G
|
XP_011519782.1:p.Phe426Cys
|
|
XM_017022094.1:c.1814T>G
|
XP_016877583.1:p.Phe605Cys
|
|
XM_017022095.1:c.1715T>G
|
XP_016877584.1:p.Phe572Cys
|
|
XM_017022096.1:c.1586T>G
|
XP_016877585.1:p.Phe529Cys
|
|
XM_017022097.1:c.1577T>G
|
XP_016877586.1:p.Phe526Cys
|
|
XM_017022098.1:c.1382T>G
|
XP_016877587.1:p.Phe461Cys
|
|
NM_002112.4:c.1709T>G
MANE Select
|
NP_002103.2:p.Phe570Cys
|
|
NM_001306146.2:c.1610T>G
|
NP_001293075.1:p.Phe537Cys
|
|