ENST00000642493.1:c.*486A>G
|
ENSP00000493524.1:n.*486A>G
|
|
ENST00000642498.1:c.846A>G
|
ENSP00000493631.1:p.Ala282=
|
|
ENST00000642538.1:c.*190A>G
|
ENSP00000493927.1:n.*190A>G
|
|
ENST00000643188.1:c.846A>G
|
ENSP00000493903.1:p.Ala282=
|
|
ENST00000643443.1:c.*553A>G
|
ENSP00000495572.1:n.*553A>G
|
|
ENST00000643502.1:c.503A>G
|
|
|
ENST00000643908.1:n.1064A>G
|
|
|
ENST00000644538.1:n.1123A>G
|
|
|
ENST00000644793.1:c.846A>G
|
ENSP00000495750.1:p.Ala282=
|
|
ENST00000645328.1:c.224A>G
|
|
|
ENST00000645408.1:c.379A>G
|
|
|
ENST00000645723.1:n.2085A>G
|
|
|
ENST00000646405.1:c.*264A>G
|
ENSP00000493744.1:n.*264A>G
|
|
ENST00000646497.1:n.791A>G
|
|
|
ENST00000646512.1:n.992A>G
|
|
|
ENST00000646735.1:c.513A>G
|
ENSP00000493763.1:p.Ala171=
|
|
ENST00000651619.1:c.846A>G
MANE Select
|
ENSP00000498303.1:p.Ala282=
|
|
ENST00000216951.6:c.846A>G
|
ENSP00000216951.2:p.Ala282=
|
|
ENST00000451957.2:c.513A>G
|
ENSP00000407517.2:p.Ala171=
|
|
NM_000178.2:c.846A>G
|
NP_000169.1:p.Ala282=
|
|
XM_005260406.3:c.846A>G
|
XP_005260463.1:p.Ala282=
|
|
XM_011528796.1:c.846A>G
|
XP_011527098.1:p.Ala282=
|
|
NM_000178.4:c.846A>G
MANE Select
|
NP_000169.1:p.Ala282=
|
|
NM_001322494.1:c.846A>G
|
NP_001309423.1:p.Ala282=
|
|
NM_001322495.1:c.846A>G
|
NP_001309424.1:p.Ala282=
|
|