ENST00000267845.8:c.1703T>G
MANE Select
|
ENSP00000267845.3:p.Phe568Cys
|
|
ENST00000267845.7:c.1703T>G
|
ENSP00000267845.3:p.Phe568Cys
|
|
ENST00000543581.5:c.1604T>G
|
ENSP00000440252.1:p.Phe535Cys
|
|
ENST00000559816.1:n.1447T>G
|
|
|
NM_001306146.1:c.1604T>G
|
NP_001293075.1:p.Phe535Cys
|
|
NM_002112.3:c.1703T>G
|
NP_002103.2:p.Phe568Cys
|
|
XM_011521479.1:c.1466T>G
|
XP_011519781.1:p.Phe489Cys
|
|
XM_011521480.1:c.1271T>G
|
XP_011519782.1:p.Phe424Cys
|
|
XM_017022094.1:c.1808T>G
|
XP_016877583.1:p.Phe603Cys
|
|
XM_017022095.1:c.1709T>G
|
XP_016877584.1:p.Phe570Cys
|
|
XM_017022096.1:c.1580T>G
|
XP_016877585.1:p.Phe527Cys
|
|
XM_017022097.1:c.1571T>G
|
XP_016877586.1:p.Phe524Cys
|
|
XM_017022098.1:c.1376T>G
|
XP_016877587.1:p.Phe459Cys
|
|
NM_002112.4:c.1703T>G
MANE Select
|
NP_002103.2:p.Phe568Cys
|
|
NM_001306146.2:c.1604T>G
|
NP_001293075.1:p.Phe535Cys
|
|