ENST00000456935.7:c.370T>G
MANE Select
|
ENSP00000395473.2:p.Phe124Val
|
|
ENST00000221363.8:c.370T>G
|
ENSP00000221363.4:p.Phe124Val
|
|
ENST00000456935.6:c.370T>G
|
ENSP00000395473.2:p.Phe124Val
|
|
ENST00000466794.5:n.352T>G
|
|
|
ENST00000486847.2:c.267T>G
|
ENSP00000470174.1:p.Ser89=
|
|
ENST00000596512.5:n.308T>G
|
|
|
ENST00000597961.1:c.361T>G
|
ENSP00000472710.1:p.Phe121Val
|
|
ENST00000598876.1:c.397T>G
|
ENSP00000470533.1:p.Phe133Val
|
|
ENST00000600281.1:n.411T>G
|
|
|
NM_000528.3:c.370T>G
|
NP_000519.2:p.Phe124Val
|
|
NM_001173498.1:c.370T>G
|
NP_001166969.1:p.Phe124Val
|
|
XM_005259913.1:c.370T>G
|
XP_005259970.1:p.Phe124Val
|
|
XM_005259913.2:c.370T>G
|
XP_005259970.1:p.Phe124Val
|
|
XM_024451518.1:c.-649T>G
|
XP_024307286.1:n.-649T>G
|
|
NM_000528.4:c.370T>G
MANE Select
|
NP_000519.2:p.Phe124Val
|
|
NM_001173498.2:c.370T>G
|
NP_001166969.1:p.Phe124Val
|
|