ENST00000588328.7:c.830T=
|
ENSP00000468516.4:p.Met277=
|
|
ENST00000651901.2:c.830T=
|
ENSP00000498922.2:p.Met277=
|
|
ENST00000698359.1:c.785T=
|
ENSP00000513682.1:p.Met262=
|
|
ENST00000698360.1:c.881T=
|
ENSP00000513683.1:p.Met294=
|
|
ENST00000698361.1:c.830T=
|
ENSP00000513684.1:p.Met277=
|
|
ENST00000698362.1:c.830T=
|
ENSP00000513685.1:p.Met277=
|
|
ENST00000698363.1:n.893T=
|
|
|
ENST00000698364.1:n.893T=
|
|
|
ENST00000698365.1:n.893T=
|
|
|
ENST00000698426.1:c.509T=
|
ENSP00000513713.1:p.Met170=
|
|
ENST00000698427.1:c.872T=
|
ENSP00000513714.1:p.Met291=
|
|
ENST00000698428.1:c.509T=
|
ENSP00000513715.1:p.Met170=
|
|
ENST00000698429.1:n.713T=
|
|
|
ENST00000698430.1:c.1080T=
|
|
|
ENST00000698431.1:c.567T=
|
ENSP00000513717.1:n.567T=
|
|
ENST00000698432.1:c.639T=
|
|
|
ENST00000698433.1:n.292T=
|
|
|
ENST00000698434.1:n.317T=
|
|
|
ENST00000698435.1:c.518T=
|
ENSP00000513719.1:p.Met173=
|
|
ENST00000244137.12:c.830T=
MANE Select
|
ENSP00000244137.5:p.Met277=
|
|
ENST00000588328.6:c.819T=
|
|
|
ENST00000590731.6:n.505T=
|
|
|
ENST00000651901.1:c.826T=
|
|
|
ENST00000244137.11:c.830T=
|
ENSP00000244137.5:p.Met277=
|
|
ENST00000397032.8:c.707T=
|
ENSP00000380226.3:p.Met236=
|
|
ENST00000436370.7:c.638T=
|
ENSP00000391890.2:p.Met213=
|
|
ENST00000588328.5:c.321T=
|
|
|
ENST00000588719.5:n.465T=
|
|
|
ENST00000590731.5:n.505T=
|
|
|
ENST00000593163.5:n.995T=
|
|
|
ENST00000609145.5:c.263T=
|
ENSP00000476514.1:p.Met88=
|
|
NM_000285.3:c.830T=
|
NP_000276.2:p.Met277=
|
|
NM_001166056.1:c.707T=
|
NP_001159528.1:p.Met236=
|
|
NM_001166057.1:c.638T=
|
NP_001159529.1:p.Met213=
|
|
NM_000285.4:c.830T=
MANE Select
|
NP_000276.2:p.Met277=
|
|
NM_001166056.2:c.707T=
|
NP_001159528.1:p.Met236=
|
|
NM_001166057.2:c.638T=
|
NP_001159529.1:p.Met213=
|
|