ENST00000644719.2:c.412C>T
MANE Select
|
ENSP00000496625.1:p.Pro138Ser
|
|
ENST00000418967.6:c.412C>T
|
ENSP00000408860.2:p.Pro138Ser
|
|
ENST00000435122.3:c.322C>T
|
ENSP00000415043.2:p.Pro108Ser
|
|
ENST00000464325.5:n.333C>T
|
|
|
ENST00000466779.5:c.*104C>T
|
ENSP00000417321.1:n.*104C>T
|
|
ENST00000466879.5:n.463C>T
|
|
|
ENST00000469053.5:c.*104C>T
|
ENSP00000418104.1:n.*104C>T
|
|
ENST00000471671.4:c.412C>T
|
ENSP00000418561.1:p.Pro138Ser
|
|
ENST00000478281.5:c.445C>T
|
ENSP00000419572.1:p.Pro149Ser
|
|
ENST00000479074.5:n.470C>T
|
|
|
ENST00000479730.5:n.567C>T
|
|
|
ENST00000483041.5:n.581C>T
|
|
|
ENST00000486063.5:n.592C>T
|
|
|
ENST00000488465.1:n.420C>T
|
|
|
NM_000500.7:c.412C>T
|
NP_000491.4:p.Pro138Ser
|
|
NM_001128590.3:c.322C>T
|
NP_001122062.3:p.Pro108Ser
|
|
XM_011514314.1:c.7C>T
|
XP_011512616.1:p.Pro3Ser
|
|
NM_000500.9:c.412C>T
MANE Select
|
NP_000491.4:p.Pro138Ser
|
|
NM_001368143.1:c.7C>T
|
NP_001355072.1:p.Pro3Ser
|
|
NM_001368144.1:c.7C>T
|
NP_001355073.1:p.Pro3Ser
|
|
NM_001128590.4:c.322C>T
|
NP_001122062.3:p.Pro108Ser
|
|
NM_001368143.2:c.7C>T
|
NP_001355072.1:p.Pro3Ser
|
|
NM_001368144.2:c.7C>T
|
NP_001355073.1:p.Pro3Ser
|
|