ENST00000302068.9:c.1244+3A>T
MANE Select
|
ENSP00000306099.4:n.1244+3A>T
|
|
ENST00000302068.8:c.1244+3A>T
|
ENSP00000306099.4:n.1244+3A>T
|
|
ENST00000502545.5:n.939+495A>T
|
|
|
ENST00000509493.1:c.587+3A>T
|
ENSP00000426757.1:n.587+3A>T
|
|
NM_001184741.1:c.1067+3A>T
|
NP_001171670.1:n.1067+3A>T
|
|
NM_005141.4:c.1244+3A>T , LRG_558t1:c.1244+3A>T
|
NP_005132.2:n.1244+3A>T
|
|
NM_001382759.1:c.1112+3A>T
|
NP_001369688.1:n.1112+3A>T
|
|
NM_001382760.1:c.1244+3A>T
|
NP_001369689.1:n.1244+3A>T
|
|
NM_001382761.1:c.1244+3A>T
|
NP_001369690.1:n.1244+3A>T
|
|
NM_001382762.1:c.944+3A>T
|
NP_001369691.1:n.944+3A>T
|
|
NM_001382763.1:c.1235+3A>T
|
NP_001369692.1:n.1235+3A>T
|
|
NM_001382764.1:c.*18+3A>T
|
NP_001369693.1:n.*18+3A>T
|
|
NM_001382765.1:c.1220+27A>T
|
NP_001369694.1:n.1220+27A>T
|
|
NM_005141.5:c.1244+3A>T
MANE Select
|
NP_005132.2:n.1244+3A>T
|
|