ENST00000377270.8:c.358A>G
|
ENSP00000366482.4:p.Lys120Glu
|
|
ENST00000484259.3:c.583A>G
MANE Select
|
ENSP00000419243.2:p.Lys195Glu
|
|
ENST00000642330.1:c.384+19452A>G
|
ENSP00000493770.1:n.384+19452A>G
|
|
ENST00000642889.1:c.166-27189A>G
|
ENSP00000493780.1:n.166-27189A>G
|
|
ENST00000643352.1:c.482+7677A>G
|
ENSP00000496488.1:n.482+7677A>G
|
|
ENST00000643765.1:c.480+7677A>G
|
|
|
ENST00000644653.1:c.*186A>G
|
ENSP00000495217.1:n.*186A>G
|
|
ENST00000644977.1:c.*207+7677A>G
|
ENSP00000495651.1:n.*207+7677A>G
|
|
ENST00000645088.1:c.*85+7677A>G
|
ENSP00000495447.1:n.*85+7677A>G
|
|
ENST00000646862.1:c.384+19452A>G
|
ENSP00000494599.1:n.384+19452A>G
|
|
ENST00000377270.7:c.583A>G
|
ENSP00000366482.3:p.Lys195Glu
|
|
ENST00000396364.7:c.482+7677A>G
|
ENSP00000379650.3:n.482+7677A>G
|
|
ENST00000396366.6:c.591A>G
|
ENSP00000379652.2:p.Ter197=
|
|
ENST00000484259.1:c.275A>G
|
|
|
ENST00000498653.5:c.358A>G
|
ENSP00000418015.1:p.Lys120Glu
|
|
NM_000144.4:c.583A>G
|
NP_000135.2:p.Lys195Glu
|
|
NM_001161706.1:c.482+7677A>G
|
NP_001155178.1:n.482+7677A>G
|
|
NM_181425.2:c.591A>G
|
NP_852090.1:p.Ter197=
|
|
NM_000144.5:c.583A>G
MANE Select
|
NP_000135.2:p.Lys195Glu
|
|
NM_181425.3:c.591A>G
|
NP_852090.1:p.Ter197=
|
|