ENST00000263038.9:c.828+397G>C
MANE Select
|
ENSP00000263038.4:n.828+397G>C
|
|
ENST00000263038.8:c.828+397G>C
|
ENSP00000263038.4:n.828+397G>C
|
|
ENST00000396913.6:c.528+397G>C
|
ENSP00000380121.2:n.528+397G>C
|
|
ENST00000396920.7:c.777+397G>C
|
ENSP00000380126.3:n.777+397G>C
|
|
NM_001037537.1:c.528+397G>C
|
NP_001032626.1:n.528+397G>C
|
|
NM_006214.3:c.828+397G>C
|
NP_006205.1:n.828+397G>C
|
|
XM_005252469.2:c.609+397G>C
|
XP_005252526.1:n.609+397G>C
|
|
NM_001323080.1:c.528+397G>C
|
NP_001310009.1:n.528+397G>C
|
|
NM_001323082.1:c.834+397G>C
|
NP_001310011.1:n.834+397G>C
|
|
NM_001323083.1:c.564+397G>C
|
NP_001310012.1:n.564+397G>C
|
|
NM_001323084.1:c.534+397G>C
|
NP_001310013.1:n.534+397G>C
|
|
NM_006214.4:c.828+397G>C
MANE Select
|
NP_006205.1:n.828+397G>C
|
|
NM_001037537.2:c.528+397G>C
|
NP_001032626.1:n.528+397G>C
|
|
NM_001323080.2:c.528+397G>C
|
NP_001310009.1:n.528+397G>C
|
|
NM_001323082.2:c.834+397G>C
|
NP_001310011.1:n.834+397G>C
|
|
NM_001323083.2:c.564+397G>C
|
NP_001310012.1:n.564+397G>C
|
|
NM_001323084.2:c.534+397G>C
|
NP_001310013.1:n.534+397G>C
|
|