ENST00000215743.8:c.1076-40G>T
MANE Select
|
ENSP00000215743.3:n.1076-40G>T
|
|
ENST00000215743.7:c.1076-40G>T
|
ENSP00000215743.3:n.1076-40G>T
|
|
ENST00000434318.1:c.837G>T
|
|
|
ENST00000437086.5:c.1028-182G>T
|
ENSP00000408070.1:n.1028-182G>T
|
|
ENST00000465385.5:n.2660-40G>T
|
|
|
ENST00000480185.1:n.113-40G>T
|
|
|
ENST00000488363.1:n.147-40G>T
|
|
|
ENST00000493132.1:n.470-40G>T
|
|
|
NM_005940.3:c.1076-40G>T
|
NP_005931.2:n.1076-40G>T
|
|
NM_005940.4:c.1076-40G>T
|
NP_005931.2:n.1076-40G>T
|
|
NR_133013.1:n.1080-182G>T
|
|
|
NM_005940.5:c.1076-40G>T
MANE Select
|
NP_005931.2:n.1076-40G>T
|
|
NR_133013.2:n.1050-182G>T
|
|
|