ENST00000321612.8:c.2202+329C>G
MANE Select
|
ENSP00000370737.4:n.2202+329C>G
|
|
ENST00000638233.1:n.637+329C>G
|
|
|
ENST00000638661.1:c.402+329C>G
|
ENSP00000491369.1:n.402+329C>G
|
|
ENST00000638694.1:n.389+329C>G
|
|
|
ENST00000639318.1:c.402+329C>G
|
ENSP00000491932.1:n.402+329C>G
|
|
ENST00000639364.1:n.1902+329C>G
|
|
|
ENST00000639443.1:n.1770+329C>G
|
|
|
ENST00000639954.1:n.1910+329C>G
|
|
|
ENST00000640505.1:n.441+329C>G
|
|
|
ENST00000321612.6:c.2202+329C>G
|
ENSP00000370737.3:n.2202+329C>G
|
|
NM_000170.2:c.2202+329C>G , LRG_643t1:c.2202+329C>G
|
NP_000161.2:n.2202+329C>G
|
|
NM_000170.3:c.2202+329C>G
MANE Select
|
NP_000161.2:n.2202+329C>G
|
|