ENST00000376649.8:c.791T>A
MANE Select
|
ENSP00000365837.3:p.Leu264Gln
|
|
ENST00000322060.9:c.707T>A
|
ENSP00000324726.5:p.Leu236Gln
|
|
ENST00000376649.7:c.791T>A
|
ENSP00000365837.3:p.Leu264Gln
|
|
ENST00000443358.6:c.707T>A
|
ENSP00000392451.2:p.Leu236Gln
|
|
ENST00000535067.5:c.358-2001T>A
|
ENSP00000443969.1:n.358-2001T>A
|
|
ENST00000542167.2:c.632T>A
|
ENSP00000438948.1:p.Leu211Gln
|
|
ENST00000543754.1:n.612T>A
|
|
|
NM_001002019.2:c.707T>A
|
NP_001002019.1:p.Leu236Gln
|
|
NM_001002020.2:c.707T>A
|
NP_001002020.1:p.Leu236Gln
|
|
NM_025215.5:c.791T>A
|
NP_079491.2:p.Leu264Gln
|
|
XM_011538768.1:c.392T>A
|
XP_011537070.1:p.Leu131Gln
|
|
XM_011538768.3:c.392T>A
|
XP_011537070.1:p.Leu131Gln
|
|
XR_001748872.1:n.1246T>A
|
|
|
NM_001002019.3:c.707T>A
|
NP_001002019.1:p.Leu236Gln
|
|
NM_001002020.3:c.707T>A
|
NP_001002020.1:p.Leu236Gln
|
|
NM_025215.6:c.791T>A
MANE Select
|
NP_079491.2:p.Leu264Gln
|
|