ENST00000267845.8:c.1843T>G
MANE Select
|
ENSP00000267845.3:p.Phe615Val
|
|
ENST00000267845.7:c.1843T>G
|
ENSP00000267845.3:p.Phe615Val
|
|
ENST00000543581.5:c.1744T>G
|
ENSP00000440252.1:p.Phe582Val
|
|
ENST00000559816.1:n.1587T>G
|
|
|
NM_001306146.1:c.1744T>G
|
NP_001293075.1:p.Phe582Val
|
|
NM_002112.3:c.1843T>G
|
NP_002103.2:p.Phe615Val
|
|
XM_011521479.1:c.1606T>G
|
XP_011519781.1:p.Phe536Val
|
|
XM_011521480.1:c.1411T>G
|
XP_011519782.1:p.Phe471Val
|
|
XM_017022094.1:c.1948T>G
|
XP_016877583.1:p.Phe650Val
|
|
XM_017022095.1:c.1849T>G
|
XP_016877584.1:p.Phe617Val
|
|
XM_017022096.1:c.1720T>G
|
XP_016877585.1:p.Phe574Val
|
|
XM_017022097.1:c.1711T>G
|
XP_016877586.1:p.Phe571Val
|
|
XM_017022098.1:c.1516T>G
|
XP_016877587.1:p.Phe506Val
|
|
NM_002112.4:c.1843T>G
MANE Select
|
NP_002103.2:p.Phe615Val
|
|
NM_001306146.2:c.1744T>G
|
NP_001293075.1:p.Phe582Val
|
|