ENST00000642496.1:c.4123T>A
|
|
|
ENST00000644397.2:c.*41T>A
MANE Select
|
ENSP00000495195.1:n.*41T>A
|
|
ENST00000373965.6:c.*41T>A
|
ENSP00000363076.3:n.*41T>A
|
|
ENST00000414778.5:c.*41T>A
|
ENSP00000410304.2:n.*41T>A
|
|
ENST00000495484.5:c.*41T>A
|
ENSP00000480780.1:n.*41T>A
|
|
ENST00000614895.4:c.*41T>A
|
ENSP00000478512.1:n.*41T>A
|
|
ENST00000616114.4:c.*41T>A
|
ENSP00000483745.1:n.*41T>A
|
|
ENST00000618301.4:c.1424T>A
|
ENSP00000482780.1:n.1424T>A
|
|
ENST00000621708.4:c.*41T>A
|
ENSP00000484454.1:n.*41T>A
|
|
NM_001142771.1:c.*41T>A
|
NP_001136243.1:n.*41T>A
|
|
NM_001142772.1:c.*41T>A
|
NP_001136244.1:n.*41T>A
|
|
NM_001354420.1:c.*41T>A
|
NP_001341349.1:n.*41T>A
|
|
NM_001354429.1:c.*41T>A
|
NP_001341358.1:n.*41T>A
|
|
XR_001747192.2:n.11556T>A
|
|
|
XR_001747193.2:n.11547T>A
|
|
|
NM_001142771.2:c.*41T>A
|
NP_001136243.1:n.*41T>A
|
|
NM_001142772.2:c.*41T>A
|
NP_001136244.1:n.*41T>A
|
|
NM_001354420.2:c.*41T>A
|
NP_001341349.1:n.*41T>A
|
|
NM_001354429.2:c.*41T>A
|
NP_001341358.1:n.*41T>A
|
|
NM_001384140.1:c.*41T>A
MANE Select
|
NP_001371069.1:n.*41T>A
|
|