ENST00000644719.2:c.408G=
MANE Select
|
ENSP00000496625.1:p.Met136=
|
|
ENST00000418967.6:c.408G=
|
ENSP00000408860.2:p.Met136=
|
|
ENST00000435122.3:c.318G=
|
ENSP00000415043.2:p.Met106=
|
|
ENST00000464325.5:n.329G=
|
|
|
ENST00000466779.5:c.*100G=
|
ENSP00000417321.1:n.*100G=
|
|
ENST00000466879.5:n.459G=
|
|
|
ENST00000469053.5:c.*100G=
|
ENSP00000418104.1:n.*100G=
|
|
ENST00000471671.4:c.408G=
|
ENSP00000418561.1:p.Met136=
|
|
ENST00000478281.5:c.441G=
|
ENSP00000419572.1:p.Met147=
|
|
ENST00000479074.5:n.466G=
|
|
|
ENST00000479730.5:n.563G=
|
|
|
ENST00000483041.5:n.577G=
|
|
|
ENST00000486063.5:n.588G=
|
|
|
ENST00000488465.1:n.416G=
|
|
|
NM_000500.7:c.408G=
|
NP_000491.4:p.Met136=
|
|
NM_001128590.3:c.318G=
|
NP_001122062.3:p.Met106=
|
|
XM_011514314.1:c.3G=
|
XP_011512616.1:p.Met1=
|
|
NM_000500.9:c.408G=
MANE Select
|
NP_000491.4:p.Met136=
|
|
NM_001368143.1:c.3G=
|
NP_001355072.1:p.Met1=
|
|
NM_001368144.1:c.3G=
|
NP_001355073.1:p.Met1=
|
|
NM_001128590.4:c.318G=
|
NP_001122062.3:p.Met106=
|
|
NM_001368143.2:c.3G=
|
NP_001355072.1:p.Met1=
|
|
NM_001368144.2:c.3G=
|
NP_001355073.1:p.Met1=
|
|