ENST00000267845.8:c.1709T>A
MANE Select
|
ENSP00000267845.3:p.Phe570Tyr
|
|
ENST00000267845.7:c.1709T>A
|
ENSP00000267845.3:p.Phe570Tyr
|
|
ENST00000543581.5:c.1610T>A
|
ENSP00000440252.1:p.Phe537Tyr
|
|
ENST00000559816.1:n.1453T>A
|
|
|
NM_001306146.1:c.1610T>A
|
NP_001293075.1:p.Phe537Tyr
|
|
NM_002112.3:c.1709T>A
|
NP_002103.2:p.Phe570Tyr
|
|
XM_011521479.1:c.1472T>A
|
XP_011519781.1:p.Phe491Tyr
|
|
XM_011521480.1:c.1277T>A
|
XP_011519782.1:p.Phe426Tyr
|
|
XM_017022094.1:c.1814T>A
|
XP_016877583.1:p.Phe605Tyr
|
|
XM_017022095.1:c.1715T>A
|
XP_016877584.1:p.Phe572Tyr
|
|
XM_017022096.1:c.1586T>A
|
XP_016877585.1:p.Phe529Tyr
|
|
XM_017022097.1:c.1577T>A
|
XP_016877586.1:p.Phe526Tyr
|
|
XM_017022098.1:c.1382T>A
|
XP_016877587.1:p.Phe461Tyr
|
|
NM_002112.4:c.1709T>A
MANE Select
|
NP_002103.2:p.Phe570Tyr
|
|
NM_001306146.2:c.1610T>A
|
NP_001293075.1:p.Phe537Tyr
|
|