ENST00000477226.6:n.767C>A
|
|
|
ENST00000683013.1:n.681C>A
|
|
|
ENST00000373960.4:c.1293C>A
MANE Select
|
ENSP00000363071.3:p.Thr431=
|
|
ENST00000373960.3:c.1293C>A
|
ENSP00000363071.3:p.Thr431=
|
|
ENST00000483395.1:n.148C>A
|
|
|
NM_001927.3:c.1293C>A , LRG_380t1:c.1293C>A
|
NP_001918.3:p.Thr431=
|
|
NM_001927.4:c.1293C>A
MANE Select
|
NP_001918.3:p.Thr431=
|
|
NM_001382708.1:c.1290C>A
|
NP_001369637.1:p.Thr430=
|
|
NM_001382709.1:c.861C>A
|
NP_001369638.1:p.Thr287=
|
|
NM_001382710.1:c.1224C>A
|
NP_001369639.1:p.Thr408=
|
|
NM_001382711.1:c.1272C>A
|
NP_001369640.1:p.Thr424=
|
|
NM_001382712.1:c.1293C>A
|
NP_001369641.1:p.Thr431=
|
|
NM_001382713.1:c.1023C>A
|
NP_001369642.1:p.Thr341=
|
|