ENST00000480188.2:n.1538+453A>T
|
|
|
ENST00000696279.1:c.4824+453A>T
|
|
|
ENST00000696280.1:n.4593+453A>T
|
|
|
ENST00000696281.1:c.4522+453A>T
|
ENSP00000512521.1:n.4522+453A>T
|
|
ENST00000697921.1:n.3382+453A>T
|
|
|
ENST00000697922.1:c.*4494+453A>T
|
ENSP00000513478.1:n.*4494+453A>T
|
|
ENST00000697923.1:n.4949+453A>T
|
|
|
ENST00000223642.3:c.4504+453A>T
MANE Select
|
ENSP00000223642.1:n.4504+453A>T
|
|
ENST00000223642.2:c.4504+453A>T
|
ENSP00000223642.1:n.4504+453A>T
|
|
ENST00000480188.1:n.37+453A>T
|
|
|
NM_001735.2:c.4504+453A>T , LRG_28t1:c.4504+453A>T
|
NP_001726.2:n.4504+453A>T
|
|
XM_011518980.1:c.4519+453A>T
|
XP_011517282.1:n.4519+453A>T
|
|
NM_001317163.1:c.4522+453A>T
|
NP_001304092.1:n.4522+453A>T
|
|
NM_001317163.2:c.4522+453A>T
|
NP_001304092.1:n.4522+453A>T
|
|
NM_001735.3:c.4504+453A>T
MANE Select
|
NP_001726.2:n.4504+453A>T
|
|