ENST00000477226.6:n.623C>A
|
|
|
ENST00000683013.1:n.537C>A
|
|
|
ENST00000373960.4:c.1149C>A
MANE Select
|
ENSP00000363071.3:p.Arg383=
|
|
ENST00000373960.3:c.1149C>A
|
ENSP00000363071.3:p.Arg383=
|
|
ENST00000477226.5:n.621C>A
|
|
|
ENST00000492726.1:n.544C>A
|
|
|
NM_001927.3:c.1149C>A , LRG_380t1:c.1149C>A
|
NP_001918.3:p.Arg383=
|
|
NM_001927.4:c.1149C>A
MANE Select
|
NP_001918.3:p.Arg383=
|
|
NM_001382708.1:c.1146C>A
|
NP_001369637.1:p.Arg382=
|
|
NM_001382709.1:c.736-19C>A
|
NP_001369638.1:n.736-19C>A
|
|
NM_001382710.1:c.1080C>A
|
NP_001369639.1:p.Arg360=
|
|
NM_001382711.1:c.1128C>A
|
NP_001369640.1:p.Arg376=
|
|
NM_001382712.1:c.1149C>A
|
NP_001369641.1:p.Arg383=
|
|
NM_001382713.1:c.879C>A
|
NP_001369642.1:p.Arg293=
|
|