ENST00000456935.7:c.346T>G
MANE Select
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ENSP00000395473.2:p.Phe116Val
|
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ENST00000221363.8:c.346T>G
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ENSP00000221363.4:p.Phe116Val
|
|
ENST00000456935.6:c.346T>G
|
ENSP00000395473.2:p.Phe116Val
|
|
ENST00000466794.5:n.328T>G
|
|
|
ENST00000486847.2:c.243T>G
|
ENSP00000470174.1:p.Ala81=
|
|
ENST00000596512.5:n.284T>G
|
|
|
ENST00000597961.1:c.337T>G
|
ENSP00000472710.1:p.Phe113Val
|
|
ENST00000598876.1:c.373T>G
|
ENSP00000470533.1:p.Phe125Val
|
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ENST00000600281.1:n.387T>G
|
|
|
NM_000528.3:c.346T>G
|
NP_000519.2:p.Phe116Val
|
|
NM_001173498.1:c.346T>G
|
NP_001166969.1:p.Phe116Val
|
|
XM_005259913.1:c.346T>G
|
XP_005259970.1:p.Phe116Val
|
|
XM_005259913.2:c.346T>G
|
XP_005259970.1:p.Phe116Val
|
|
XM_024451518.1:c.-673T>G
|
XP_024307286.1:n.-673T>G
|
|
NM_000528.4:c.346T>G
MANE Select
|
NP_000519.2:p.Phe116Val
|
|
NM_001173498.2:c.346T>G
|
NP_001166969.1:p.Phe116Val
|
|