ENST00000644719.2:c.1361C>G
MANE Select
|
ENSP00000496625.1:p.Pro454Arg
|
|
ENST00000418967.6:c.1361C>G
|
ENSP00000408860.2:p.Pro454Arg
|
|
ENST00000435122.3:c.1271C>G
|
ENSP00000415043.2:p.Pro424Arg
|
|
ENST00000479074.5:n.1502C>G
|
|
|
ENST00000479730.5:n.1477C>G
|
|
|
ENST00000483041.5:n.1530C>G
|
|
|
ENST00000486063.5:n.1340C>G
|
|
|
NM_000500.7:c.1361C>G
|
NP_000491.4:p.Pro454Arg
|
|
NM_001128590.3:c.1271C>G
|
NP_001122062.3:p.Pro424Arg
|
|
XM_011514314.1:c.956C>G
|
XP_011512616.1:p.Pro319Arg
|
|
NM_000500.9:c.1361C>G
MANE Select
|
NP_000491.4:p.Pro454Arg
|
|
NM_001368143.1:c.956C>G
|
NP_001355072.1:p.Pro319Arg
|
|
NM_001368144.1:c.956C>G
|
NP_001355073.1:p.Pro319Arg
|
|
NM_001128590.4:c.1271C>G
|
NP_001122062.3:p.Pro424Arg
|
|
NM_001368143.2:c.956C>G
|
NP_001355072.1:p.Pro319Arg
|
|
NM_001368144.2:c.956C>G
|
NP_001355073.1:p.Pro319Arg
|
|