ENST00000369733.8:c.766+11G>A
|
ENSP00000358748.3:n.766+11G>A
|
|
ENST00000648076.2:c.766+11G>A
MANE Select
|
ENSP00000497653.1:n.766+11G>A
|
|
ENST00000649118.1:n.881+11G>A
|
|
|
ENST00000650263.1:c.718+11G>A
|
ENSP00000497850.1:n.718+11G>A
|
|
ENST00000353479.9:c.766+11G>A
|
ENSP00000340937.5:n.766+11G>A
|
|
ENST00000369733.7:c.766+11G>A
|
ENSP00000358748.3:n.766+11G>A
|
|
ENST00000393211.3:c.766+11G>A
|
ENSP00000376905.3:n.766+11G>A
|
|
ENST00000488320.1:n.111+11G>A
|
|
|
NM_000494.3:c.766+11G>A
|
NP_000485.3:n.766+11G>A
|
|
NM_000494.4:c.766+11G>A
MANE Select
|
NP_000485.3:n.766+11G>A
|
|