|
NM_000494.4:c.911-12C>G
MANE Select
|
NP_000485.3:n.911-12C>G
|
|
ENST00000648076.2:c.911-12C>G
MANE Select
|
ENSP00000497653.1:n.911-12C>G
|
|
NM_000494.3:c.911-12C>G
|
NP_000485.3:n.911-12C>G
|
|
ENST00000353479.9:c.911-12C>G
|
ENSP00000340937.5:n.911-12C>G
|
|
ENST00000369733.7:c.911-12C>G
|
ENSP00000358748.3:n.911-12C>G
|
|
ENST00000369733.8:c.911-12C>G
|
ENSP00000358748.3:n.911-12C>G
|
|
ENST00000393211.3:c.911-12C>G
|
ENSP00000376905.3:n.911-12C>G
|
|
ENST00000488320.1:n.362-12C>G
|
|
|
ENST00000650263.1:c.863-12C>G
|
ENSP00000497850.1:n.863-12C>G
|