ENST00000348974.5:c.849+198T=
|
ENSP00000330021.7:n.849+198T=
|
|
ENST00000394236.9:c.849+198T=
MANE Select
|
ENSP00000377783.3:n.849+198T=
|
|
ENST00000407433.6:c.804+198T=
|
ENSP00000385794.2:n.804+198T=
|
|
ENST00000647936.1:c.849+198T=
|
ENSP00000496822.1:n.849+198T=
|
|
ENST00000648381.1:n.1017+198T=
|
|
|
ENST00000648853.1:c.807+198T=
|
ENSP00000497262.1:n.807+198T=
|
|
ENST00000649103.1:c.948+198T=
|
ENSP00000497962.1:n.948+198T=
|
|
ENST00000650591.1:c.945+198T=
|
ENSP00000497376.1:n.945+198T=
|
|
ENST00000394236.7:c.849+198T=
|
ENSP00000377783.3:n.849+198T=
|
|
ENST00000407433.5:c.456+198T=
|
ENSP00000385794.1:n.456+198T=
|
|
NM_000313.3:c.849+198T= , LRG_572t1:c.849+198T=
|
NP_000304.2:n.849+198T=
|
|
NM_001314077.1:c.945+198T= , LRG_572t2:c.945+198T=
|
NP_001301006.1:n.945+198T=
|
|
NM_000313.4:c.849+198T=
MANE Select
|
NP_000304.2:n.849+198T=
|
|
NM_001314077.2:c.945+198T=
|
NP_001301006.1:n.945+198T=
|
|