ENST00000644719.2:c.1025G=
MANE Select
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ENSP00000496625.1:p.Arg342=
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|
ENST00000418967.6:c.1025G=
|
ENSP00000408860.2:p.Arg342=
|
|
ENST00000435122.3:c.935G=
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ENSP00000415043.2:p.Arg312=
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|
ENST00000479074.5:n.1083G=
|
|
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ENST00000479730.5:n.1141G=
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|
|
ENST00000483041.5:n.1194G=
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|
|
ENST00000486063.5:n.1004G=
|
|
|
NM_000500.7:c.1025G=
|
NP_000491.4:p.Arg342=
|
|
NM_001128590.3:c.935G=
|
NP_001122062.3:p.Arg312=
|
|
XM_011514314.1:c.620G=
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XP_011512616.1:p.Arg207=
|
|
NM_000500.9:c.1025G=
MANE Select
|
NP_000491.4:p.Arg342=
|
|
NM_001368143.1:c.620G=
|
NP_001355072.1:p.Arg207=
|
|
NM_001368144.1:c.620G=
|
NP_001355073.1:p.Arg207=
|
|
NM_001128590.4:c.935G=
|
NP_001122062.3:p.Arg312=
|
|
NM_001368143.2:c.620G=
|
NP_001355072.1:p.Arg207=
|
|
NM_001368144.2:c.620G=
|
NP_001355073.1:p.Arg207=
|
|