ENST00000269980.7:c.779T>C
MANE Select
|
ENSP00000269980.2:p.Ile260Thr
|
|
ENST00000269980.6:c.779T>C
|
ENSP00000269980.2:p.Ile260Thr
|
|
ENST00000457836.6:c.713T>C
|
ENSP00000416000.2:p.Ile238Thr
|
|
ENST00000535632.5:n.408T>C
|
|
|
ENST00000540732.3:c.881T>C
|
ENSP00000443246.1:p.Ile294Thr
|
|
ENST00000542943.5:c.692T>C
|
ENSP00000440345.1:p.Ile231Thr
|
|
ENST00000545787.1:n.407T>C
|
|
|
ENST00000595085.5:c.779T>C
|
ENSP00000471150.2:p.Ile260Thr
|
|
NM_000709.3:c.779T>C
|
NP_000700.1:p.Ile260Thr
|
|
NM_001164783.1:c.779T>C
|
NP_001158255.1:p.Ile260Thr
|
|
NM_000709.4:c.779T>C
MANE Select
|
NP_000700.1:p.Ile260Thr
|
|
NM_001164783.2:c.779T>C
|
NP_001158255.1:p.Ile260Thr
|
|