ENST00000269980.7:c.1010G>C
MANE Select
|
ENSP00000269980.2:p.Ser337Thr
|
|
ENST00000269980.6:c.1010G>C
|
ENSP00000269980.2:p.Ser337Thr
|
|
ENST00000457836.6:c.1019G>C
|
ENSP00000416000.2:p.Ser340Thr
|
|
ENST00000540732.3:c.1112G>C
|
ENSP00000443246.1:p.Ser371Thr
|
|
ENST00000542943.5:c.923G>C
|
ENSP00000440345.1:p.Ser308Thr
|
|
ENST00000595085.5:c.922+315G>C
|
ENSP00000471150.2:n.922+315G>C
|
|
NM_000709.3:c.1010G>C
|
NP_000700.1:p.Ser337Thr
|
|
NM_001164783.1:c.1007G>C
|
NP_001158255.1:p.Ser336Thr
|
|
NM_000709.4:c.1010G>C
MANE Select
|
NP_000700.1:p.Ser337Thr
|
|
NM_001164783.2:c.1007G>C
|
NP_001158255.1:p.Ser336Thr
|
|