ENST00000216117.9:c.23+429G>T
MANE Select
|
ENSP00000216117.8:n.23+429G>T
|
|
ENST00000481190.2:c.156+296G>T
|
ENSP00000503987.1:n.156+296G>T
|
|
ENST00000677931.1:c.23+429G>T
|
ENSP00000502849.1:n.23+429G>T
|
|
ENST00000679074.1:c.23+429G>T
|
ENSP00000503459.1:n.23+429G>T
|
|
ENST00000216117.8:c.23+429G>T
|
ENSP00000216117.8:n.23+429G>T
|
|
ENST00000412893.5:c.23+429G>T
|
ENSP00000413316.1:n.23+429G>T
|
|
ENST00000481190.1:n.237+296G>T
|
|
|
NM_002133.2:c.23+429G>T
|
NP_002124.1:n.23+429G>T
|
|
NM_002133.3:c.23+429G>T
MANE Select
|
NP_002124.1:n.23+429G>T
|
|