ENST00000696170.1:c.*183+128A>T
|
ENSP00000512461.1:n.*183+128A>T
|
|
ENST00000696171.1:c.578+128A>T
|
ENSP00000512462.1:n.578+128A>T
|
|
ENST00000696172.1:c.338-2686A>T
|
ENSP00000512463.1:n.338-2686A>T
|
|
ENST00000378588.5:c.674+128A>T
MANE Select
|
ENSP00000367851.4:n.674+128A>T
|
|
ENST00000378588.4:c.674+128A>T
|
ENSP00000367851.4:n.674+128A>T
|
|
ENST00000465127.1:c.171+370269A>T
|
ENSP00000417050.1:n.171+370269A>T
|
|
NM_000397.3:c.674+128A>T , LRG_53t1:c.674+128A>T
|
NP_000388.2:n.674+128A>T
|
|
XM_011543890.1:c.368+128A>T
|
XP_011542192.1:n.368+128A>T
|
|
NM_000397.4:c.674+128A>T
MANE Select
|
NP_000388.2:n.674+128A>T
|
|