ENST00000525748.6:c.1886T>C
MANE Select
|
ENSP00000434364.2:p.Phe629Ser
|
|
ENST00000298923.11:c.*1183T>C
|
ENSP00000298923.7:n.*1183T>C
|
|
ENST00000525748.5:c.1886T>C
|
ENSP00000434364.1:p.Phe629Ser
|
|
ENST00000528440.1:n.417T>C
|
|
|
NM_004211.3:c.1886T>C
|
NP_004202.2:p.Phe629Ser
|
|
XM_005253225.1:c.1184T>C
|
XP_005253282.1:p.Phe395Ser
|
|
XM_011520473.1:c.1886T>C
|
XP_011518775.1:p.Phe629Ser
|
|
NM_001318369.1:c.1184T>C
|
NP_001305298.1:p.Phe395Ser
|
|
NM_004211.4:c.1886T>C
|
NP_004202.3:p.Phe629Ser
|
|
XM_017018544.2:c.1010T>C
|
XP_016874033.1:p.Phe337Ser
|
|
XM_017018545.2:c.845T>C
|
XP_016874034.1:p.Phe282Ser
|
|
NM_001318369.2:c.1184T>C
|
NP_001305298.1:p.Phe395Ser
|
|
NM_004211.5:c.1886T>C
MANE Select
|
NP_004202.4:p.Phe629Ser
|
|