ENST00000456935.7:c.404C>G
MANE Select
|
ENSP00000395473.2:p.Thr135Arg
|
|
ENST00000221363.8:c.404C>G
|
ENSP00000221363.4:p.Thr135Arg
|
|
ENST00000456935.6:c.404C>G
|
ENSP00000395473.2:p.Thr135Arg
|
|
ENST00000466794.5:n.386C>G
|
|
|
ENST00000486847.2:c.301C>G
|
ENSP00000470174.1:p.His101Asp
|
|
ENST00000596512.5:n.342C>G
|
|
|
ENST00000597961.1:c.395C>G
|
ENSP00000472710.1:p.Thr132Arg
|
|
ENST00000598876.1:c.431C>G
|
ENSP00000470533.1:p.Thr144Arg
|
|
ENST00000600281.1:n.445C>G
|
|
|
NM_000528.3:c.404C>G
|
NP_000519.2:p.Thr135Arg
|
|
NM_001173498.1:c.404C>G
|
NP_001166969.1:p.Thr135Arg
|
|
XM_005259913.1:c.404C>G
|
XP_005259970.1:p.Thr135Arg
|
|
XM_005259913.2:c.404C>G
|
XP_005259970.1:p.Thr135Arg
|
|
XM_024451518.1:c.-615C>G
|
XP_024307286.1:n.-615C>G
|
|
NM_000528.4:c.404C>G
MANE Select
|
NP_000519.2:p.Thr135Arg
|
|
NM_001173498.2:c.404C>G
|
NP_001166969.1:p.Thr135Arg
|
|