ENST00000302804.12:c.614A>C
MANE Select
|
ENSP00000302898.6:p.Tyr205Ser
|
|
ENST00000302804.11:c.614A>C
|
ENSP00000302898.6:p.Tyr205Ser
|
|
ENST00000415300.6:c.557A>C
|
ENSP00000407162.1:p.Tyr186Ser
|
|
ENST00000448930.5:c.509A>C
|
ENSP00000406798.2:p.Tyr170Ser
|
|
ENST00000594599.1:c.98A>C
|
ENSP00000469894.1:p.Tyr33Ser
|
|
ENST00000596375.1:c.*175A>C
|
ENSP00000470465.1:n.*175A>C
|
|
ENST00000598785.5:c.512A>C
|
ENSP00000471830.1:p.Tyr171Ser
|
|
ENST00000599062.5:c.605A>C
|
ENSP00000469983.1:p.Tyr202Ser
|
|
ENST00000601799.5:c.*913A>C
|
ENSP00000468918.1:n.*913A>C
|
|
NM_001015878.1:c.614A>C
|
NP_001015878.1:p.Tyr205Ser
|
|
NM_001015879.1:c.557A>C
|
NP_001015879.1:p.Tyr186Ser
|
|
NM_003160.2:c.512A>C
|
NP_003151.2:p.Tyr171Ser
|
|
XR_430209.2:n.1508A>C
|
|
|
XR_430209.3:n.1551A>C
|
|
|
NM_001015878.2:c.614A>C
MANE Select
|
NP_001015878.1:p.Tyr205Ser
|
|
NM_001015879.2:c.557A>C
|
NP_001015879.1:p.Tyr186Ser
|
|
NM_003160.3:c.512A>C
|
NP_003151.2:p.Tyr171Ser
|
|