ENST00000348974.5:c.1956T>G
|
ENSP00000330021.7:p.Asp652Glu
|
|
ENST00000394236.9:c.1956T>G
MANE Select
|
ENSP00000377783.3:p.Asp652Glu
|
|
ENST00000407433.6:c.1911T>G
|
ENSP00000385794.2:p.Asp637Glu
|
|
ENST00000647936.1:c.*59T>G
|
ENSP00000496822.1:n.*59T>G
|
|
ENST00000648381.1:n.2124T>G
|
|
|
ENST00000648853.1:c.1914T>G
|
ENSP00000497262.1:p.Asp638Glu
|
|
ENST00000650591.1:c.2052T>G
|
ENSP00000497376.1:p.Asp684Glu
|
|
ENST00000394236.7:c.1956T>G
|
ENSP00000377783.3:p.Asp652Glu
|
|
ENST00000407433.5:c.1563T>G
|
ENSP00000385794.1:p.Asp521Glu
|
|
NM_000313.3:c.1956T>G , LRG_572t1:c.1956T>G
|
NP_000304.2:p.Asp652Glu
|
|
NM_001314077.1:c.2052T>G , LRG_572t2:c.2052T>G
|
NP_001301006.1:p.Asp684Glu
|
|
NM_000313.4:c.1956T>G
MANE Select
|
NP_000304.2:p.Asp652Glu
|
|
NM_001314077.2:c.2052T>G
|
NP_001301006.1:p.Asp684Glu
|
|