ENST00000559133.6:c.*378+128A>G
|
ENSP00000453958.2:n.*378+128A>G
|
|
ENST00000674301.2:c.*1083+128A>G
|
ENSP00000501333.2:n.*1083+128A>G
|
|
ENST00000682170.1:n.1751+128A>G
|
|
|
ENST00000682767.1:n.867+128A>G
|
|
|
ENST00000316623.10:c.7570+128A>G
MANE Select
|
ENSP00000325527.5:n.7570+128A>G
|
|
ENST00000674301.1:c.2736+128A>G
|
ENSP00000501333.1:n.2736+128A>G
|
|
ENST00000316623.9:c.7570+128A>G
|
ENSP00000325527.5:n.7570+128A>G
|
|
ENST00000559133.5:c.2939+128A>G
|
|
|
NM_000138.4:c.7570+128A>G , LRG_778t1:c.7570+128A>G
|
NP_000129.3:n.7570+128A>G
|
|
NM_000138.5:c.7570+128A>G
MANE Select
|
NP_000129.3:n.7570+128A>G
|
|