ENST00000636937.2:c.1886A>G
|
ENSP00000516154.1:p.Asp629Gly
|
|
ENST00000268124.11:c.1886A>G
MANE Select
|
ENSP00000268124.5:p.Asp629Gly
|
|
ENST00000530292.3:c.1487A>G
|
ENSP00000432885.2:p.Asp496Gly
|
|
ENST00000635986.2:c.1886A>G
|
ENSP00000490653.2:p.Asp629Gly
|
|
ENST00000636774.1:c.*453A>G
|
ENSP00000489799.1:n.*453A>G
|
|
ENST00000637238.1:c.623A>G
|
ENSP00000490756.1:p.Asp208Gly
|
|
ENST00000637264.1:c.958A>G
|
|
|
ENST00000666746.1:c.1463A>G
|
|
|
ENST00000670281.1:c.206A>G
|
ENSP00000499709.1:p.Asp69Gly
|
|
ENST00000672071.1:n.2084A>G
|
|
|
ENST00000672923.2:n.1989A>G
|
|
|
ENST00000268124.9:c.1886A>G
|
ENSP00000268124.5:p.Asp629Gly
|
|
ENST00000442287.6:c.1886A>G
|
ENSP00000399851.2:p.Asp629Gly
|
|
ENST00000526314.2:c.268A>G
|
|
|
ENST00000526398.1:c.75A>G
|
|
|
ENST00000532584.5:n.88A>G
|
|
|
ENST00000631044.2:c.*1269A>G
|
ENSP00000486730.1:n.*1269A>G
|
|
NM_001126131.1:c.1886A>G
|
NP_001119603.1:p.Asp629Gly
|
|
NM_002693.2:c.1886A>G
|
NP_002684.1:p.Asp629Gly
|
|
NM_001126131.2:c.1886A>G
|
NP_001119603.1:p.Asp629Gly
|
|
NM_002693.3:c.1886A>G
MANE Select
|
NP_002684.1:p.Asp629Gly
|
|