ENST00000452035.7:n.2296A>T
|
|
|
ENST00000483004.2:c.1593A>T
|
ENSP00000419887.2:p.Thr531=
|
|
ENST00000698628.1:c.1625-246A>T
|
ENSP00000513848.1:n.1625-246A>T
|
|
ENST00000698629.1:n.2081A>T
|
|
|
ENST00000698630.1:n.2525A>T
|
|
|
ENST00000698631.1:n.2526A>T
|
|
|
ENST00000698632.1:n.3415A>T
|
|
|
ENST00000698633.1:n.3305A>T
|
|
|
ENST00000425368.7:c.1809A>T
MANE Select
|
ENSP00000416561.2:p.Thr603=
|
|
ENST00000425368.6:c.1809A>T
|
ENSP00000416561.2:p.Thr603=
|
|
ENST00000456570.5:c.3315A>T
|
ENSP00000410815.1:p.Thr1105=
|
|
ENST00000467360.1:n.935A>T
|
|
|
ENST00000477310.1:c.2862A>T
|
ENSP00000418996.1:p.Thr954=
|
|
ENST00000482312.1:n.25A>T
|
|
|
ENST00000483004.1:c.431A>T
|
|
|
NM_001710.5:c.1809A>T , LRG_136t1:c.1809A>T
|
NP_001701.2:p.Thr603=
|
|
NM_001710.6:c.1809A>T
MANE Select
|
NP_001701.2:p.Thr603=
|
|