ENST00000340850.10:c.511A>G
|
ENSP00000344570.5:p.Ile171Val
|
|
ENST00000377728.8:c.511A>G
MANE Select
|
ENSP00000366957.3:p.Ile171Val
|
|
ENST00000377740.5:c.511A>G
|
ENSP00000366969.4:p.Ile171Val
|
|
ENST00000377748.6:c.685A>G
|
ENSP00000366977.2:p.Ile229Val
|
|
ENST00000400913.6:c.511A>G
|
ENSP00000383704.1:p.Ile171Val
|
|
ENST00000400915.8:c.622A>G
|
ENSP00000383706.4:p.Ile208Val
|
|
ENST00000489097.6:n.987A>G
|
|
|
ENST00000535355.6:c.718A>G
|
ENSP00000441445.1:p.Ile240Val
|
|
ENST00000537245.6:c.622A>G
|
ENSP00000439625.2:p.Ile208Val
|
|
ENST00000673471.2:c.808A>G
|
ENSP00000500749.1:p.Ile270Val
|
|
ENST00000674790.1:c.*723A>G
|
ENSP00000502815.1:n.*723A>G
|
|
ENST00000675123.1:c.511A>G
|
ENSP00000502132.1:p.Ile171Val
|
|
ENST00000675548.1:c.*339A>G
|
ENSP00000502684.1:n.*339A>G
|
|
ENST00000675694.1:c.511A>G
|
ENSP00000501925.1:p.Ile171Val
|
|
ENST00000340850.9:c.511A>G
|
ENSP00000344570.5:p.Ile171Val
|
|
ENST00000377725.5:c.511A>G
|
ENSP00000366954.1:p.Ile171Val
|
|
ENST00000377728.7:c.511A>G
|
ENSP00000366957.3:p.Ile171Val
|
|
ENST00000377732.5:c.622A>G
|
ENSP00000366961.1:p.Ile208Val
|
|
ENST00000377740.4:c.742A>G
|
ENSP00000366969.3:p.Ile248Val
|
|
ENST00000377748.5:c.742A>G
|
ENSP00000366977.1:p.Ile248Val
|
|
ENST00000400913.5:c.511A>G
|
ENSP00000383704.1:p.Ile171Val
|
|
ENST00000400915.7:c.679A>G
|
ENSP00000383706.3:p.Ile227Val
|
|
ENST00000489097.5:n.987A>G
|
|
|
ENST00000535355.5:c.718A>G
|
ENSP00000441445.1:p.Ile240Val
|
|
ENST00000537245.5:c.748A>G
|
ENSP00000439625.1:p.Ile250Val
|
|
NM_001042663.1:c.679A>G
|
NP_001036128.1:p.Ile227Val
|
|
NM_001042664.1:c.511A>G
|
NP_001036129.1:p.Ile171Val
|
|
NM_001042665.1:c.511A>G
|
NP_001036130.1:p.Ile171Val
|
|
NM_001265592.1:c.748A>G
|
NP_001252521.1:p.Ile250Val
|
|
NM_001265593.1:c.718A>G
|
NP_001252522.1:p.Ile240Val
|
|
NM_001265594.1:c.511A>G
|
NP_001252523.1:p.Ile171Val
|
|
NM_020631.4:c.511A>G
|
NP_065682.2:p.Ile171Val
|
|
NM_198681.3:c.742A>G
|
NP_941374.2:p.Ile248Val
|
|
NM_001042663.2:c.679A>G
|
NP_001036128.1:p.Ile227Val
|
|
NM_001265594.2:c.511A>G
|
NP_001252523.1:p.Ile171Val
|
|
NM_020631.5:c.511A>G
|
NP_065682.2:p.Ile171Val
|
|
NM_001042663.3:c.622A>G
|
NP_001036128.2:p.Ile208Val
|
|
NM_001265592.2:c.622A>G
|
NP_001252521.2:p.Ile208Val
|
|
NM_020631.6:c.511A>G
MANE Select
|
NP_065682.2:p.Ile171Val
|
|
NM_198681.4:c.511A>G
|
NP_941374.3:p.Ile171Val
|
|