ENST00000267845.8:c.1844T>A
MANE Select
|
ENSP00000267845.3:p.Phe615Tyr
|
|
ENST00000267845.7:c.1844T>A
|
ENSP00000267845.3:p.Phe615Tyr
|
|
ENST00000543581.5:c.1745T>A
|
ENSP00000440252.1:p.Phe582Tyr
|
|
ENST00000559816.1:n.1588T>A
|
|
|
NM_001306146.1:c.1745T>A
|
NP_001293075.1:p.Phe582Tyr
|
|
NM_002112.3:c.1844T>A
|
NP_002103.2:p.Phe615Tyr
|
|
XM_011521479.1:c.1607T>A
|
XP_011519781.1:p.Phe536Tyr
|
|
XM_011521480.1:c.1412T>A
|
XP_011519782.1:p.Phe471Tyr
|
|
XM_017022094.1:c.1949T>A
|
XP_016877583.1:p.Phe650Tyr
|
|
XM_017022095.1:c.1850T>A
|
XP_016877584.1:p.Phe617Tyr
|
|
XM_017022096.1:c.1721T>A
|
XP_016877585.1:p.Phe574Tyr
|
|
XM_017022097.1:c.1712T>A
|
XP_016877586.1:p.Phe571Tyr
|
|
XM_017022098.1:c.1517T>A
|
XP_016877587.1:p.Phe506Tyr
|
|
NM_002112.4:c.1844T>A
MANE Select
|
NP_002103.2:p.Phe615Tyr
|
|
NM_001306146.2:c.1745T>A
|
NP_001293075.1:p.Phe582Tyr
|
|