ENST00000269980.7:c.1025G>C
MANE Select
|
ENSP00000269980.2:p.Ser342Thr
|
|
ENST00000269980.6:c.1025G>C
|
ENSP00000269980.2:p.Ser342Thr
|
|
ENST00000457836.6:c.1034G>C
|
ENSP00000416000.2:p.Ser345Thr
|
|
ENST00000540732.3:c.1127G>C
|
ENSP00000443246.1:p.Ser376Thr
|
|
ENST00000542943.5:c.938G>C
|
ENSP00000440345.1:p.Ser313Thr
|
|
ENST00000595085.5:c.922+330G>C
|
ENSP00000471150.2:n.922+330G>C
|
|
NM_000709.3:c.1025G>C
|
NP_000700.1:p.Ser342Thr
|
|
NM_001164783.1:c.1022G>C
|
NP_001158255.1:p.Ser341Thr
|
|
NM_000709.4:c.1025G>C
MANE Select
|
NP_000700.1:p.Ser342Thr
|
|
NM_001164783.2:c.1022G>C
|
NP_001158255.1:p.Ser341Thr
|
|