ENST00000376033.3:c.6334-9G>C
MANE Select
|
ENSP00000365201.2:n.6334-9G>C
|
|
ENST00000376007.8:c.6334-9G>C
|
ENSP00000365175.4:n.6334-9G>C
|
|
ENST00000376033.2:c.6334-9G>C
|
ENSP00000365201.2:n.6334-9G>C
|
|
ENST00000462617.1:n.681G>C
|
|
|
ENST00000482441.1:n.394-9G>C
|
|
|
ENST00000492691.5:n.784G>C
|
|
|
NM_004638.3:c.6334-9G>C
|
NP_004629.3:n.6334-9G>C
|
|
NM_080686.2:c.6334-9G>C
|
NP_542417.2:n.6334-9G>C
|
|
XM_011514890.1:c.6121-9G>C
|
XP_011513192.1:n.6121-9G>C
|
|
XM_017011274.1:c.6121-9G>C
|
XP_016866763.1:n.6121-9G>C
|
|
NM_004638.4:c.6334-9G>C
MANE Select
|
NP_004629.3:n.6334-9G>C
|
|
NM_080686.3:c.6334-9G>C
|
NP_542417.2:n.6334-9G>C
|
|