ENST00000477226.6:n.217G=
|
|
|
ENST00000683013.1:n.131G=
|
|
|
ENST00000373960.4:c.743G=
MANE Select
|
ENSP00000363071.3:p.Arg248=
|
|
ENST00000373960.3:c.743G=
|
ENSP00000363071.3:p.Arg248=
|
|
ENST00000477226.5:n.215G=
|
|
|
ENST00000492726.1:n.138G=
|
|
|
NM_001927.3:c.743G= , LRG_380t1:c.743G=
|
NP_001918.3:p.Arg248=
|
|
NM_001927.4:c.743G=
MANE Select
|
NP_001918.3:p.Arg248=
|
|
NM_001382708.1:c.740G=
|
NP_001369637.1:p.Arg247=
|
|
NM_001382709.1:c.735+156G=
|
NP_001369638.1:n.735+156G=
|
|
NM_001382710.1:c.743G=
|
NP_001369639.1:p.Arg248=
|
|
NM_001382711.1:c.743G=
|
NP_001369640.1:p.Arg248=
|
|
NM_001382712.1:c.743G=
|
NP_001369641.1:p.Arg248=
|
|
NM_001382713.1:c.496-23G=
|
NP_001369642.1:n.496-23G=
|
|