ENST00000477226.6:n.863A>T
|
|
|
ENST00000683013.1:n.777A>T
|
|
|
ENST00000373960.4:c.1389A>T
MANE Select
|
ENSP00000363071.3:p.Thr463=
|
|
ENST00000373960.3:c.1389A>T
|
ENSP00000363071.3:p.Thr463=
|
|
ENST00000483395.1:n.244A>T
|
|
|
NM_001927.3:c.1389A>T , LRG_380t1:c.1389A>T
|
NP_001918.3:p.Thr463=
|
|
NM_001927.4:c.1389A>T
MANE Select
|
NP_001918.3:p.Thr463=
|
|
NM_001382708.1:c.1386A>T
|
NP_001369637.1:p.Thr462=
|
|
NM_001382709.1:c.957A>T
|
NP_001369638.1:p.Thr319=
|
|
NM_001382710.1:c.1320A>T
|
NP_001369639.1:p.Thr440=
|
|
NM_001382711.1:c.1368A>T
|
NP_001369640.1:p.Thr456=
|
|
NM_001382712.1:c.1371+221A>T
|
NP_001369641.1:n.1371+221A>T
|
|
NM_001382713.1:c.1119A>T
|
NP_001369642.1:p.Thr373=
|
|