ENST00000267845.8:c.1842C>G
MANE Select
|
ENSP00000267845.3:p.Ile614Met
|
|
ENST00000267845.7:c.1842C>G
|
ENSP00000267845.3:p.Ile614Met
|
|
ENST00000543581.5:c.1743C>G
|
ENSP00000440252.1:p.Ile581Met
|
|
ENST00000559816.1:n.1586C>G
|
|
|
NM_001306146.1:c.1743C>G
|
NP_001293075.1:p.Ile581Met
|
|
NM_002112.3:c.1842C>G
|
NP_002103.2:p.Ile614Met
|
|
XM_011521479.1:c.1605C>G
|
XP_011519781.1:p.Ile535Met
|
|
XM_011521480.1:c.1410C>G
|
XP_011519782.1:p.Ile470Met
|
|
XM_017022094.1:c.1947C>G
|
XP_016877583.1:p.Ile649Met
|
|
XM_017022095.1:c.1848C>G
|
XP_016877584.1:p.Ile616Met
|
|
XM_017022096.1:c.1719C>G
|
XP_016877585.1:p.Ile573Met
|
|
XM_017022097.1:c.1710C>G
|
XP_016877586.1:p.Ile570Met
|
|
XM_017022098.1:c.1515C>G
|
XP_016877587.1:p.Ile505Met
|
|
NM_002112.4:c.1842C>G
MANE Select
|
NP_002103.2:p.Ile614Met
|
|
NM_001306146.2:c.1743C>G
|
NP_001293075.1:p.Ile581Met
|
|