ENST00000319555.8:c.40+8694T>A
MANE Select
|
ENSP00000326630.2:n.40+8694T>A
|
|
ENST00000319555.7:c.40+8694T>A
|
ENSP00000326630.2:n.40+8694T>A
|
|
ENST00000562417.1:n.73+8694T>A
|
|
|
ENST00000562437.2:c.40+8694T>A
|
ENSP00000480412.1:n.40+8694T>A
|
|
ENST00000563351.5:c.40+8694T>A
|
ENSP00000484216.1:n.40+8694T>A
|
|
ENST00000569086.5:c.40+8694T>A
|
ENSP00000482796.1:n.40+8694T>A
|
|
NM_153813.2:c.40+8694T>A
|
NP_722520.2:n.40+8694T>A
|
|
XM_011522914.1:c.139+10434T>A
|
XP_011521216.1:n.139+10434T>A
|
|
XM_011522916.1:c.87+10434T>A
|
XP_011521218.1:n.87+10434T>A
|
|
XM_011522918.1:c.-15+10743T>A
|
XP_011521220.1:n.-15+10743T>A
|
|
XM_011522914.2:c.139+10434T>A
|
XP_011521216.1:n.139+10434T>A
|
|
NM_153813.3:c.40+8694T>A
MANE Select
|
NP_722520.2:n.40+8694T>A
|
|