ENST00000246337.9:c.1000A>G
MANE Select
|
ENSP00000246337.4:p.Ile334Val
|
|
ENST00000491773.6:c.757A>G
|
ENSP00000498551.1:p.Ile253Val
|
|
ENST00000636293.1:c.862A>G
|
ENSP00000490710.1:p.Ile288Val
|
|
ENST00000636836.1:c.*36A>G
|
ENSP00000490594.1:n.*36A>G
|
|
ENST00000651476.1:c.895A>G
|
ENSP00000498668.1:p.Ile299Val
|
|
ENST00000652165.1:c.757A>G
|
ENSP00000498295.1:p.Ile253Val
|
|
ENST00000652287.1:c.937A>G
|
ENSP00000498413.1:p.Ile313Val
|
|
ENST00000652514.1:c.961A>G
|
ENSP00000498635.1:n.961A>G
|
|
ENST00000246337.8:c.1000A>G
|
ENSP00000246337.4:p.Ile334Val
|
|
ENST00000465678.1:n.745A>G
|
|
|
ENST00000472254.1:n.753A>G
|
|
|
ENST00000494399.5:n.1667A>G
|
|
|
NM_000374.4:c.1000A>G
|
NP_000365.3:p.Ile334Val
|
|
NR_036510.1:n.1183A>G
|
|
|
XM_005271169.1:c.784A>G
|
XP_005271226.1:p.Ile262Val
|
|
XM_005271170.1:c.784A>G
|
XP_005271227.1:p.Ile262Val
|
|
XM_011542080.1:c.937A>G
|
XP_011540382.1:p.Ile313Val
|
|
XM_011542081.1:c.832A>G
|
XP_011540383.1:p.Ile278Val
|
|
NM_000374.5:c.1000A>G
MANE Select
|
NP_000365.3:p.Ile334Val
|
|
NR_158184.1:n.1081A>G
|
|
|
NR_158185.1:n.1031A>G
|
|
|
NR_036510.2:n.1062A>G
|
|
|