ENST00000427990.6:c.372G=
|
ENSP00000391302.2:p.Met124=
|
|
ENST00000433768.6:c.*134G=
|
ENSP00000392514.1:n.*134G=
|
|
ENST00000438034.6:c.459G=
|
ENSP00000404525.2:p.Met153=
|
|
ENST00000397278.8:c.372G=
MANE Select
|
ENSP00000380448.4:p.Met124=
|
|
ENST00000319136.8:c.420G=
|
ENSP00000317674.4:p.Met140=
|
|
ENST00000397278.7:c.372G=
|
ENSP00000380448.3:p.Met124=
|
|
ENST00000397279.8:c.372G=
|
ENSP00000380449.4:p.Met124=
|
|
ENST00000422706.5:c.372G=
|
ENSP00000411507.1:p.Met124=
|
|
ENST00000426053.5:c.318G=
|
ENSP00000388477.1:p.Met106=
|
|
ENST00000427990.5:c.372G=
|
ENSP00000391302.1:p.Met124=
|
|
NM_001136540.1:c.372G=
|
NP_001130012.1:p.Met124=
|
|
NM_001136541.1:c.318G=
|
NP_001130013.1:p.Met106=
|
|
NM_003661.3:c.372G=
|
NP_003652.2:p.Met124=
|
|
NM_145343.2:c.420G= , LRG_169t1:c.420G=
|
NP_663318.1:p.Met140=
|
|
XM_005261796.2:c.318G=
|
XP_005261853.1:p.Met106=
|
|
XM_011530478.1:c.9G=
|
XP_011528780.1:p.Met3=
|
|
NM_001362927.1:c.318G=
|
NP_001349856.1:p.Met106=
|
|
XM_011530478.2:c.9G=
|
XP_011528780.1:p.Met3=
|
|
NM_001362927.2:c.318G=
|
NP_001349856.1:p.Met106=
|
|
NM_003661.4:c.372G=
MANE Select
|
NP_003652.2:p.Met124=
|
|
NM_001136540.2:c.372G=
|
NP_001130012.1:p.Met124=
|
|
NM_001136541.2:c.318G=
|
NP_001130013.1:p.Met106=
|
|
NM_145343.3:c.420G=
|
NP_663318.1:p.Met140=
|
|