ENST00000696170.1:c.*407-194A>G
|
ENSP00000512461.1:n.*407-194A>G
|
|
ENST00000696171.1:c.802-194A>G
|
ENSP00000512462.1:n.802-194A>G
|
|
ENST00000378588.5:c.898-194A>G
MANE Select
|
ENSP00000367851.4:n.898-194A>G
|
|
ENST00000378588.4:c.898-194A>G
|
ENSP00000367851.4:n.898-194A>G
|
|
ENST00000465127.1:c.171+377683A>G
|
ENSP00000417050.1:n.171+377683A>G
|
|
ENST00000492288.1:n.323-194A>G
|
|
|
NM_000397.3:c.898-194A>G , LRG_53t1:c.898-194A>G
|
NP_000388.2:n.898-194A>G
|
|
XM_011543890.1:c.592-194A>G
|
XP_011542192.1:n.592-194A>G
|
|
NM_000397.4:c.898-194A>G
MANE Select
|
NP_000388.2:n.898-194A>G
|
|