ENST00000348974.5:c.669T>C
|
ENSP00000330021.7:p.Asp223=
|
|
ENST00000394236.9:c.669T>C
MANE Select
|
ENSP00000377783.3:p.Asp223=
|
|
ENST00000407433.6:c.624T>C
|
ENSP00000385794.2:p.Asp208=
|
|
ENST00000647936.1:c.669T>C
|
ENSP00000496822.1:p.Asp223=
|
|
ENST00000648381.1:n.837T>C
|
|
|
ENST00000648853.1:c.627T>C
|
ENSP00000497262.1:p.Asp209=
|
|
ENST00000649103.1:c.768T>C
|
ENSP00000497962.1:n.768T>C
|
|
ENST00000650591.1:c.765T>C
|
ENSP00000497376.1:p.Asp255=
|
|
ENST00000394236.7:c.669T>C
|
ENSP00000377783.3:p.Asp223=
|
|
ENST00000407433.5:c.276T>C
|
ENSP00000385794.1:p.Asp92=
|
|
NM_000313.3:c.669T>C , LRG_572t1:c.669T>C
|
NP_000304.2:p.Asp223=
|
|
NM_001314077.1:c.765T>C , LRG_572t2:c.765T>C
|
NP_001301006.1:p.Asp255=
|
|
NM_000313.4:c.669T>C
MANE Select
|
NP_000304.2:p.Asp223=
|
|
NM_001314077.2:c.765T>C
|
NP_001301006.1:p.Asp255=
|
|