ENST00000477226.6:n.567G=
|
|
|
ENST00000683013.1:n.481G=
|
|
|
ENST00000373960.4:c.1093G=
MANE Select
|
ENSP00000363071.3:p.Asp365=
|
|
ENST00000373960.3:c.1093G=
|
ENSP00000363071.3:p.Asp365=
|
|
ENST00000477226.5:n.565G=
|
|
|
ENST00000492726.1:n.488G=
|
|
|
NM_001927.3:c.1093G= , LRG_380t1:c.1093G=
|
NP_001918.3:p.Asp365=
|
|
NM_001927.4:c.1093G=
MANE Select
|
NP_001918.3:p.Asp365=
|
|
NM_001382708.1:c.1090G=
|
NP_001369637.1:p.Asp364=
|
|
NM_001382709.1:c.736-75G=
|
NP_001369638.1:n.736-75G=
|
|
NM_001382710.1:c.1024G=
|
NP_001369639.1:p.Asp342=
|
|
NM_001382711.1:c.1072G=
|
NP_001369640.1:p.Asp358=
|
|
NM_001382712.1:c.1093G=
|
NP_001369641.1:p.Asp365=
|
|
NM_001382713.1:c.823G=
|
NP_001369642.1:p.Asp275=
|
|