ENST00000480188.2:n.1510T>C
|
|
|
ENST00000696279.1:c.4796T>C
|
|
|
ENST00000696280.1:n.4565T>C
|
|
|
ENST00000696281.1:c.4494T>C
|
ENSP00000512521.1:p.Thr1498=
|
|
ENST00000697921.1:n.3354T>C
|
|
|
ENST00000697922.1:c.*4466T>C
|
ENSP00000513478.1:n.*4466T>C
|
|
ENST00000697923.1:n.4921T>C
|
|
|
ENST00000223642.3:c.4476T>C
MANE Select
|
ENSP00000223642.1:p.Thr1492=
|
|
ENST00000223642.2:c.4476T>C
|
ENSP00000223642.1:p.Thr1492=
|
|
ENST00000480188.1:n.9T>C
|
|
|
NM_001735.2:c.4476T>C , LRG_28t1:c.4476T>C
|
NP_001726.2:p.Thr1492=
|
|
XM_011518980.1:c.4491T>C
|
XP_011517282.1:p.Thr1497=
|
|
NM_001317163.1:c.4494T>C
|
NP_001304092.1:p.Thr1498=
|
|
NM_001317163.2:c.4494T>C
|
NP_001304092.1:p.Thr1498=
|
|
NM_001735.3:c.4476T>C
MANE Select
|
NP_001726.2:p.Thr1492=
|
|