ENST00000376649.8:c.784T>C
MANE Select
|
ENSP00000365837.3:p.Tyr262His
|
|
ENST00000322060.9:c.700T>C
|
ENSP00000324726.5:p.Tyr234His
|
|
ENST00000376649.7:c.784T>C
|
ENSP00000365837.3:p.Tyr262His
|
|
ENST00000443358.6:c.700T>C
|
ENSP00000392451.2:p.Tyr234His
|
|
ENST00000535067.5:c.358-2008T>C
|
ENSP00000443969.1:n.358-2008T>C
|
|
ENST00000542167.2:c.625T>C
|
ENSP00000438948.1:p.Tyr209His
|
|
ENST00000543754.1:n.605T>C
|
|
|
NM_001002019.2:c.700T>C
|
NP_001002019.1:p.Tyr234His
|
|
NM_001002020.2:c.700T>C
|
NP_001002020.1:p.Tyr234His
|
|
NM_025215.5:c.784T>C
|
NP_079491.2:p.Tyr262His
|
|
XM_011538768.1:c.385T>C
|
XP_011537070.1:p.Tyr129His
|
|
XM_011538768.3:c.385T>C
|
XP_011537070.1:p.Tyr129His
|
|
XR_001748872.1:n.1239T>C
|
|
|
NM_001002019.3:c.700T>C
|
NP_001002019.1:p.Tyr234His
|
|
NM_001002020.3:c.700T>C
|
NP_001002020.1:p.Tyr234His
|
|
NM_025215.6:c.784T>C
MANE Select
|
NP_079491.2:p.Tyr262His
|
|