ENST00000452035.7:n.2165T>C
|
|
|
ENST00000483004.2:c.1557T>C
|
ENSP00000419887.2:p.Thr519=
|
|
ENST00000698628.1:c.1624+364T>C
|
ENSP00000513848.1:n.1624+364T>C
|
|
ENST00000698629.1:n.1950T>C
|
|
|
ENST00000698630.1:n.2489T>C
|
|
|
ENST00000698631.1:n.2490T>C
|
|
|
ENST00000698632.1:n.3284T>C
|
|
|
ENST00000698633.1:n.3174T>C
|
|
|
ENST00000698636.1:n.1995T>C
|
|
|
ENST00000425368.7:c.1773T>C
MANE Select
|
ENSP00000416561.2:p.Thr591=
|
|
ENST00000425368.6:c.1773T>C
|
ENSP00000416561.2:p.Thr591=
|
|
ENST00000456570.5:c.3279T>C
|
ENSP00000410815.1:p.Thr1093=
|
|
ENST00000467360.1:n.899T>C
|
|
|
ENST00000477310.1:c.2826T>C
|
ENSP00000418996.1:p.Thr942=
|
|
ENST00000483004.1:c.395T>C
|
|
|
NM_001710.5:c.1773T>C , LRG_136t1:c.1773T>C
|
NP_001701.2:p.Thr591=
|
|
NM_001710.6:c.1773T>C
MANE Select
|
NP_001701.2:p.Thr591=
|
|