ENST00000289575.10:c.1463G>C
MANE Select
|
ENSP00000289575.5:p.Ser488Thr
|
|
ENST00000289575.9:c.1463G>C
|
ENSP00000289575.5:p.Ser488Thr
|
|
ENST00000428359.6:c.1397G>C
|
ENSP00000388912.2:p.Ser466Thr
|
|
ENST00000454962.6:c.782G>C
|
ENSP00000389653.2:p.Ser261Thr
|
|
ENST00000525650.5:c.1031G>C
|
ENSP00000436324.1:p.Ser344Thr
|
|
ENST00000528108.1:n.269G>C
|
|
|
ENST00000530012.1:n.290G>C
|
|
|
ENST00000531756.5:n.1010G>C
|
|
|
ENST00000532236.5:c.1115G>C
|
ENSP00000434112.1:p.Ser372Thr
|
|
NM_001145211.2:c.1397G>C
|
NP_001138683.1:p.Ser466Thr
|
|
NM_001145212.2:c.1031G>C
|
NP_001138684.1:p.Ser344Thr
|
|
NM_007256.4:c.1463G>C
|
NP_009187.1:p.Ser488Thr
|
|
XM_017017157.1:c.1469G>C
|
XP_016872646.1:p.Ser490Thr
|
|
NM_001145211.3:c.1397G>C
|
NP_001138683.1:p.Ser466Thr
|
|
NM_001145212.3:c.1031G>C
|
NP_001138684.1:p.Ser344Thr
|
|
NM_007256.5:c.1463G>C
MANE Select
|
NP_009187.1:p.Ser488Thr
|
|