ENST00000477226.6:n.567G>T
|
|
|
ENST00000683013.1:n.481G>T
|
|
|
ENST00000373960.4:c.1093G>T
MANE Select
|
ENSP00000363071.3:p.Asp365Tyr
|
|
ENST00000373960.3:c.1093G>T
|
ENSP00000363071.3:p.Asp365Tyr
|
|
ENST00000477226.5:n.565G>T
|
|
|
ENST00000492726.1:n.488G>T
|
|
|
NM_001927.3:c.1093G>T , LRG_380t1:c.1093G>T
|
NP_001918.3:p.Asp365Tyr
|
|
NM_001927.4:c.1093G>T
MANE Select
|
NP_001918.3:p.Asp365Tyr
|
|
NM_001382708.1:c.1090G>T
|
NP_001369637.1:p.Asp364Tyr
|
|
NM_001382709.1:c.736-75G>T
|
NP_001369638.1:n.736-75G>T
|
|
NM_001382710.1:c.1024G>T
|
NP_001369639.1:p.Asp342Tyr
|
|
NM_001382711.1:c.1072G>T
|
NP_001369640.1:p.Asp358Tyr
|
|
NM_001382712.1:c.1093G>T
|
NP_001369641.1:p.Asp365Tyr
|
|
NM_001382713.1:c.823G>T
|
NP_001369642.1:p.Asp275Tyr
|
|