ENST00000321612.8:c.2202+382C>T
MANE Select
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ENSP00000370737.4:n.2202+382C>T
|
|
ENST00000638233.1:n.637+382C>T
|
|
|
ENST00000638661.1:c.402+382C>T
|
ENSP00000491369.1:n.402+382C>T
|
|
ENST00000638694.1:n.389+382C>T
|
|
|
ENST00000639318.1:c.402+382C>T
|
ENSP00000491932.1:n.402+382C>T
|
|
ENST00000639364.1:n.1902+382C>T
|
|
|
ENST00000639443.1:n.1770+382C>T
|
|
|
ENST00000639954.1:n.1910+382C>T
|
|
|
ENST00000640505.1:n.441+382C>T
|
|
|
ENST00000321612.6:c.2202+382C>T
|
ENSP00000370737.3:n.2202+382C>T
|
|
NM_000170.2:c.2202+382C>T , LRG_643t1:c.2202+382C>T
|
NP_000161.2:n.2202+382C>T
|
|
NM_000170.3:c.2202+382C>T
MANE Select
|
NP_000161.2:n.2202+382C>T
|
|