ENST00000559133.6:c.*378+121A>T
|
ENSP00000453958.2:n.*378+121A>T
|
|
ENST00000674301.2:c.*1083+121A>T
|
ENSP00000501333.2:n.*1083+121A>T
|
|
ENST00000682170.1:n.1751+121A>T
|
|
|
ENST00000682767.1:n.867+121A>T
|
|
|
ENST00000316623.10:c.7570+121A>T
MANE Select
|
ENSP00000325527.5:n.7570+121A>T
|
|
ENST00000674301.1:c.2736+121A>T
|
ENSP00000501333.1:n.2736+121A>T
|
|
ENST00000316623.9:c.7570+121A>T
|
ENSP00000325527.5:n.7570+121A>T
|
|
ENST00000559133.5:c.2939+121A>T
|
|
|
NM_000138.4:c.7570+121A>T , LRG_778t1:c.7570+121A>T
|
NP_000129.3:n.7570+121A>T
|
|
NM_000138.5:c.7570+121A>T
MANE Select
|
NP_000129.3:n.7570+121A>T
|
|