ENST00000524717.6:c.514-39963T>A
MANE Select
|
ENSP00000434552.1:n.514-39963T>A
|
|
ENST00000524717.5:c.514-39963T>A
|
ENSP00000434552.1:n.514-39963T>A
|
|
NM_032427.3:c.514-39963T>A
|
NP_115803.1:n.514-39963T>A
|
|
XM_011543023.1:c.73-39963T>A
|
XP_011541325.1:n.73-39963T>A
|
|
XM_011543024.1:c.-171-39963T>A
|
XP_011541326.1:n.-171-39963T>A
|
|
XM_011543025.1:c.514-39963T>A
|
XP_011541327.1:n.514-39963T>A
|
|
XM_011543023.3:c.73-39963T>A
|
XP_011541325.1:n.73-39963T>A
|
|
XM_011543024.3:c.-171-39963T>A
|
XP_011541326.1:n.-171-39963T>A
|
|
XM_011543025.2:c.514-39963T>A
|
XP_011541327.1:n.514-39963T>A
|
|
NM_032427.4:c.514-39963T>A
MANE Select
|
NP_115803.1:n.514-39963T>A
|
|