ENST00000526189.3:c.541G=
|
ENSP00000488104.2:p.Asp181=
|
|
ENST00000533357.5:c.622G=
MANE Select
|
ENSP00000432943.1:p.Asp208=
|
|
ENST00000672287.2:c.34G=
|
ENSP00000499818.2:p.Asp12=
|
|
ENST00000672602.2:c.622G=
|
ENSP00000500814.2:p.Asp208=
|
|
ENST00000674861.1:n.685G=
|
|
|
ENST00000463290.5:c.622G=
|
ENSP00000431538.1:p.Asp208=
|
|
ENST00000476410.1:n.82G=
|
|
|
ENST00000488271.1:n.60G=
|
|
|
ENST00000491222.5:c.34G=
|
ENSP00000431441.1:p.Asp12=
|
|
ENST00000526189.2:c.285G=
|
|
|
ENST00000533357.4:c.622G=
|
ENSP00000432943.1:p.Asp208=
|
|
NM_000530.6:c.622G= , LRG_256t1:c.622G=
|
NP_000521.2:p.Asp208=
|
|
NM_000530.7:c.622G=
|
NP_000521.2:p.Asp208=
|
|
NM_001315491.1:c.622G=
|
NP_001302420.1:p.Asp208=
|
|
XM_017001321.2:c.652G=
|
XP_016856810.1:p.Asp218=
|
|
NM_000530.8:c.622G=
MANE Select
|
NP_000521.2:p.Asp208=
|
|
NM_001315491.2:c.622G=
|
NP_001302420.1:p.Asp208=
|
|