ENST00000456935.7:c.379T>C
MANE Select
|
ENSP00000395473.2:p.Trp127Arg
|
|
ENST00000221363.8:c.379T>C
|
ENSP00000221363.4:p.Trp127Arg
|
|
ENST00000456935.6:c.379T>C
|
ENSP00000395473.2:p.Trp127Arg
|
|
ENST00000466794.5:n.361T>C
|
|
|
ENST00000486847.2:c.276T>C
|
ENSP00000470174.1:p.Val92=
|
|
ENST00000596512.5:n.317T>C
|
|
|
ENST00000597961.1:c.370T>C
|
ENSP00000472710.1:p.Trp124Arg
|
|
ENST00000598876.1:c.406T>C
|
ENSP00000470533.1:p.Trp136Arg
|
|
ENST00000600281.1:n.420T>C
|
|
|
NM_000528.3:c.379T>C
|
NP_000519.2:p.Trp127Arg
|
|
NM_001173498.1:c.379T>C
|
NP_001166969.1:p.Trp127Arg
|
|
XM_005259913.1:c.379T>C
|
XP_005259970.1:p.Trp127Arg
|
|
XM_005259913.2:c.379T>C
|
XP_005259970.1:p.Trp127Arg
|
|
XM_024451518.1:c.-640T>C
|
XP_024307286.1:n.-640T>C
|
|
NM_000528.4:c.379T>C
MANE Select
|
NP_000519.2:p.Trp127Arg
|
|
NM_001173498.2:c.379T>C
|
NP_001166969.1:p.Trp127Arg
|
|