ENST00000357685.11:c.434T>C
MANE Select
|
ENSP00000350314.5:p.Phe145Ser
|
|
ENST00000357685.9:c.434T>C
|
ENSP00000350314.5:p.Phe145Ser
|
|
ENST00000361053.8:c.434T>C
|
ENSP00000354338.4:p.Phe145Ser
|
|
ENST00000438022.5:c.332T>C
|
ENSP00000414843.1:p.Phe111Ser
|
|
ENST00000460924.6:n.526T>C
|
|
|
ENST00000494860.5:n.286T>C
|
|
|
ENST00000525468.1:n.423T>C
|
|
|
ENST00000525987.5:n.777T>C
|
|
|
ENST00000526088.5:c.332T>C
|
ENSP00000436615.1:p.Phe111Ser
|
|
ENST00000527939.1:c.*76T>C
|
ENSP00000436956.1:n.*76T>C
|
|
ENST00000530677.1:c.141T>C
|
|
|
ENST00000531169.5:c.332T>C
|
ENSP00000437053.1:p.Phe111Ser
|
|
ENST00000532593.5:c.119T>C
|
ENSP00000431802.1:p.Phe40Ser
|
|
ENST00000532612.5:c.364T>C
|
|
|
ENST00000534122.5:n.1049T>C
|
|
|
ENST00000534550.5:c.*76T>C
|
ENSP00000434488.1:n.*76T>C
|
|
NM_001037290.2:c.332T>C
|
NP_001032367.2:p.Phe111Ser
|
|
NM_001256397.1:c.332T>C
|
NP_001243326.1:p.Phe111Ser
|
|
NM_001256398.1:c.434T>C
|
NP_001243327.1:p.Phe145Ser
|
|
NM_001256400.1:c.119T>C
|
NP_001243329.1:p.Phe40Ser
|
|
NM_031938.5:c.434T>C
|
NP_114144.4:p.Phe145Ser
|
|
NM_001037290.3:c.332T>C
|
NP_001032367.3:p.Phe111Ser
|
|
NM_001256397.2:c.332T>C
|
NP_001243326.2:p.Phe111Ser
|
|
NM_001256398.2:c.434T>C
|
NP_001243327.2:p.Phe145Ser
|
|
NM_001256400.2:c.119T>C
|
NP_001243329.2:p.Phe40Ser
|
|
NM_031938.7:c.434T>C
MANE Select
|
NP_114144.5:p.Phe145Ser
|
|
NM_001037290.4:c.332T>C
|
NP_001032367.3:p.Phe111Ser
|
|
NM_001256397.3:c.332T>C
|
NP_001243326.2:p.Phe111Ser
|
|
NM_001256398.3:c.434T>C
|
NP_001243327.2:p.Phe145Ser
|
|
NM_001256400.3:c.119T>C
|
NP_001243329.2:p.Phe40Ser
|
|