ENST00000578493.2:n.954+133G>T
|
|
|
ENST00000699291.1:c.746+133G>T
|
ENSP00000514272.1:n.746+133G>T
|
|
ENST00000699292.1:n.794G>T
|
|
|
ENST00000225275.4:c.1621+133G>T
MANE Select
|
ENSP00000225275.3:n.1621+133G>T
|
|
ENST00000225275.3:c.1621+133G>T
|
ENSP00000225275.3:n.1621+133G>T
|
|
ENST00000577220.1:c.79+133G>T
|
ENSP00000464668.1:n.79+133G>T
|
|
NM_000250.1:c.1621+133G>T , LRG_84t1:c.1621+133G>T
|
NP_000241.1:n.1621+133G>T
|
|
XM_011524821.1:c.1807+133G>T
|
XP_011523123.1:n.1807+133G>T
|
|
XM_011524822.1:c.1336+133G>T
|
XP_011523124.1:n.1336+133G>T
|
|
NM_000250.2:c.1621+133G>T
MANE Select
|
NP_000241.1:n.1621+133G>T
|
|