ENST00000348974.5:c.1851A>G
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ENSP00000330021.7:p.Thr617=
|
|
ENST00000394236.9:c.1851A>G
MANE Select
|
ENSP00000377783.3:p.Thr617=
|
|
ENST00000407433.6:c.1806A>G
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ENSP00000385794.2:p.Thr602=
|
|
ENST00000647936.1:c.1644+2178A>G
|
ENSP00000496822.1:n.1644+2178A>G
|
|
ENST00000648381.1:n.2019A>G
|
|
|
ENST00000648853.1:c.1809A>G
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ENSP00000497262.1:p.Thr603=
|
|
ENST00000650591.1:c.1947A>G
|
ENSP00000497376.1:p.Thr649=
|
|
ENST00000394236.7:c.1851A>G
|
ENSP00000377783.3:p.Thr617=
|
|
ENST00000407433.5:c.1458A>G
|
ENSP00000385794.1:p.Thr486=
|
|
NM_000313.3:c.1851A>G , LRG_572t1:c.1851A>G
|
NP_000304.2:p.Thr617=
|
|
NM_001314077.1:c.1947A>G , LRG_572t2:c.1947A>G
|
NP_001301006.1:p.Thr649=
|
|
NM_000313.4:c.1851A>G
MANE Select
|
NP_000304.2:p.Thr617=
|
|
NM_001314077.2:c.1947A>G
|
NP_001301006.1:p.Thr649=
|
|