ENST00000227322.8:c.1179+795G>T
MANE Select
|
ENSP00000227322.3:n.1179+795G>T
|
|
ENST00000227322.7:c.1179+795G>T
|
ENSP00000227322.3:n.1179+795G>T
|
|
ENST00000429220.5:c.958+795G>T
|
|
|
ENST00000444935.5:c.1092-1526G>T
|
|
|
NM_003904.3:c.1179+795G>T
|
NP_003895.1:n.1179+795G>T
|
|
NM_001317086.1:c.1017+795G>T
|
NP_001304015.1:n.1017+795G>T
|
|
NM_003904.4:c.1179+795G>T
|
NP_003895.1:n.1179+795G>T
|
|
XR_001748023.2:n.2507+795G>T
|
|
|
NM_003904.5:c.1179+795G>T
MANE Select
|
NP_003895.1:n.1179+795G>T
|
|
NM_001317086.2:c.1017+795G>T
|
NP_001304015.1:n.1017+795G>T
|
|