ENST00000477226.6:n.846G=
|
|
|
ENST00000683013.1:n.760G=
|
|
|
ENST00000373960.4:c.1372G=
MANE Select
|
ENSP00000363071.3:p.Val458=
|
|
ENST00000373960.3:c.1372G=
|
ENSP00000363071.3:p.Val458=
|
|
ENST00000483395.1:n.227G=
|
|
|
NM_001927.3:c.1372G= , LRG_380t1:c.1372G=
|
NP_001918.3:p.Val458=
|
|
NM_001927.4:c.1372G=
MANE Select
|
NP_001918.3:p.Val458=
|
|
NM_001382708.1:c.1369G=
|
NP_001369637.1:p.Val457=
|
|
NM_001382709.1:c.940G=
|
NP_001369638.1:p.Val314=
|
|
NM_001382710.1:c.1303G=
|
NP_001369639.1:p.Val435=
|
|
NM_001382711.1:c.1351G=
|
NP_001369640.1:p.Val451=
|
|
NM_001382712.1:c.1371+204G=
|
NP_001369641.1:n.1371+204G=
|
|
NM_001382713.1:c.1102G=
|
NP_001369642.1:p.Val368=
|
|