ENST00000348974.5:c.2029T>G
|
ENSP00000330021.7:p.Ter677Glu
|
|
ENST00000394236.9:c.2029T>G
MANE Select
|
ENSP00000377783.3:p.Ter677Glu
|
|
ENST00000407433.6:c.1984T>G
|
ENSP00000385794.2:p.Ter662Glu
|
|
ENST00000647936.1:c.*132T>G
|
ENSP00000496822.1:n.*132T>G
|
|
ENST00000648381.1:n.2197T>G
|
|
|
ENST00000648853.1:c.1987T>G
|
ENSP00000497262.1:p.Ter663Glu
|
|
ENST00000650591.1:c.2125T>G
|
ENSP00000497376.1:p.Ter709Glu
|
|
ENST00000394236.7:c.2029T>G
|
ENSP00000377783.3:p.Ter677Glu
|
|
ENST00000407433.5:c.1636T>G
|
ENSP00000385794.1:p.Ter546Glu
|
|
NM_000313.3:c.2029T>G , LRG_572t1:c.2029T>G
|
NP_000304.2:p.Ter677Glu
|
|
NM_001314077.1:c.2125T>G , LRG_572t2:c.2125T>G
|
NP_001301006.1:p.Ter709Glu
|
|
NM_000313.4:c.2029T>G
MANE Select
|
NP_000304.2:p.Ter677Glu
|
|
NM_001314077.2:c.2125T>G
|
NP_001301006.1:p.Ter709Glu
|
|