ENST00000644719.2:c.665C>G
MANE Select
|
ENSP00000496625.1:p.Pro222Arg
|
|
ENST00000418967.6:c.665C>G
|
ENSP00000408860.2:p.Pro222Arg
|
|
ENST00000435122.3:c.575C>G
|
ENSP00000415043.2:p.Pro192Arg
|
|
ENST00000462278.1:n.354C>G
|
|
|
ENST00000466779.5:c.*357C>G
|
ENSP00000417321.1:n.*357C>G
|
|
ENST00000466879.5:n.716C>G
|
|
|
ENST00000479074.5:n.723C>G
|
|
|
ENST00000479730.5:n.781C>G
|
|
|
ENST00000483041.5:n.834C>G
|
|
|
ENST00000486063.5:n.845C>G
|
|
|
NM_000500.7:c.665C>G
|
NP_000491.4:p.Pro222Arg
|
|
NM_001128590.3:c.575C>G
|
NP_001122062.3:p.Pro192Arg
|
|
XM_011514314.1:c.260C>G
|
XP_011512616.1:p.Pro87Arg
|
|
NM_000500.9:c.665C>G
MANE Select
|
NP_000491.4:p.Pro222Arg
|
|
NM_001368143.1:c.260C>G
|
NP_001355072.1:p.Pro87Arg
|
|
NM_001368144.1:c.260C>G
|
NP_001355073.1:p.Pro87Arg
|
|
NM_001128590.4:c.575C>G
|
NP_001122062.3:p.Pro192Arg
|
|
NM_001368143.2:c.260C>G
|
NP_001355072.1:p.Pro87Arg
|
|
NM_001368144.2:c.260C>G
|
NP_001355073.1:p.Pro87Arg
|
|