ENST00000502274.2:c.3374+226T>C
|
|
|
ENST00000515425.6:c.3478+226T>C
MANE Select
|
ENSP00000423660.1:n.3478+226T>C
|
|
ENST00000675793.1:c.*2988T>C
|
ENSP00000502039.1:n.*2988T>C
|
|
ENST00000323829.9:c.*2866+226T>C
|
ENSP00000313025.5:n.*2866+226T>C
|
|
ENST00000504517.5:c.3008+226T>C
|
ENSP00000421779.1:n.3008+226T>C
|
|
ENST00000504690.5:c.3478+226T>C
|
ENSP00000425627.1:n.3478+226T>C
|
|
ENST00000510779.1:c.2528+226T>C
|
|
|
ENST00000512049.5:c.3457+226T>C
|
ENSP00000421860.1:n.3457+226T>C
|
|
ENST00000515229.5:n.140+226T>C
|
|
|
ENST00000515425.5:c.3478+226T>C
|
ENSP00000423660.1:n.3478+226T>C
|
|
NM_024577.3:c.3478+226T>C , LRG_269t1:c.3478+226T>C
|
NP_078853.2:n.3478+226T>C
|
|
NM_024577.4:c.3478+226T>C
MANE Select
|
NP_078853.2:n.3478+226T>C
|
|