ENST00000477226.6:n.837G>T
|
|
|
ENST00000683013.1:n.751G>T
|
|
|
ENST00000373960.4:c.1363G>T
MANE Select
|
ENSP00000363071.3:p.Asp455Tyr
|
|
ENST00000373960.3:c.1363G>T
|
ENSP00000363071.3:p.Asp455Tyr
|
|
ENST00000483395.1:n.218G>T
|
|
|
NM_001927.3:c.1363G>T , LRG_380t1:c.1363G>T
|
NP_001918.3:p.Asp455Tyr
|
|
NM_001927.4:c.1363G>T
MANE Select
|
NP_001918.3:p.Asp455Tyr
|
|
NM_001382708.1:c.1360G>T
|
NP_001369637.1:p.Asp454Tyr
|
|
NM_001382709.1:c.931G>T
|
NP_001369638.1:p.Asp311Tyr
|
|
NM_001382710.1:c.1294G>T
|
NP_001369639.1:p.Asp432Tyr
|
|
NM_001382711.1:c.1342G>T
|
NP_001369640.1:p.Asp448Tyr
|
|
NM_001382712.1:c.1363G>T
|
NP_001369641.1:p.Asp455Tyr
|
|
NM_001382713.1:c.1093G>T
|
NP_001369642.1:p.Asp365Tyr
|
|