ENST00000269217.11:c.1412T>C
MANE Plus Clinical
|
ENSP00000269217.5:p.Phe471Ser
|
|
ENST00000313654.14:c.6239T>C
MANE Select
|
ENSP00000324532.8:p.Phe2080Ser
|
|
ENST00000649721.1:c.3131T>C
|
ENSP00000497885.1:p.Phe1044Ser
|
|
ENST00000269217.10:c.1412T>C
|
ENSP00000269217.5:p.Phe471Ser
|
|
ENST00000313654.13:c.6239T>C
|
ENSP00000324532.8:p.Phe2080Ser
|
|
ENST00000399516.7:c.6071T>C
|
ENSP00000382432.2:p.Phe2024Ser
|
|
ENST00000586751.5:c.1017T>C
|
|
|
ENST00000587184.5:c.1244T>C
|
ENSP00000466557.1:p.Phe415Ser
|
|
ENST00000588770.5:n.817T>C
|
|
|
NM_000227.4:c.1412T>C
|
NP_000218.3:p.Phe471Ser
|
|
NM_001127717.2:c.6071T>C
|
NP_001121189.2:p.Phe2024Ser
|
|
NM_001127718.2:c.1244T>C
|
NP_001121190.2:p.Phe415Ser
|
|
NM_198129.2:c.6239T>C
|
NP_937762.2:p.Phe2080Ser
|
|
XM_011525978.1:c.6266T>C
|
XP_011524280.1:p.Phe2089Ser
|
|
XM_011525979.1:c.6257T>C
|
XP_011524281.1:p.Phe2086Ser
|
|
XM_011525980.1:c.6248T>C
|
XP_011524282.1:p.Phe2083Ser
|
|
XM_011525981.1:c.6134T>C
|
XP_011524283.1:p.Phe2045Ser
|
|
XM_011525982.1:c.6266T>C
|
XP_011524284.1:p.Phe2089Ser
|
|
XM_011525978.2:c.6266T>C
|
XP_011524280.1:p.Phe2089Ser
|
|
XM_011525979.2:c.6257T>C
|
XP_011524281.1:p.Phe2086Ser
|
|
XM_011525980.2:c.6248T>C
|
XP_011524282.1:p.Phe2083Ser
|
|
XM_011525981.2:c.6134T>C
|
XP_011524283.1:p.Phe2045Ser
|
|
XM_011525982.2:c.6266T>C
|
XP_011524284.1:p.Phe2089Ser
|
|
XM_017025743.1:c.4118T>C
|
XP_016881232.1:p.Phe1373Ser
|
|
XM_017025744.1:c.1808T>C
|
XP_016881233.1:p.Phe603Ser
|
|
XR_001753199.1:n.6507T>C
|
|
|
NM_000227.5:c.1412T>C
|
NP_000218.3:p.Phe471Ser
|
|
NM_001127717.3:c.6071T>C
|
NP_001121189.2:p.Phe2024Ser
|
|
NM_001127718.3:c.1244T>C
|
NP_001121190.2:p.Phe415Ser
|
|
NM_198129.3:c.6239T>C
|
NP_937762.2:p.Phe2080Ser
|
|
NM_000227.6:c.1412T>C
MANE Plus Clinical
|
NP_000218.3:p.Phe471Ser
|
|
NM_001127717.4:c.6071T>C
|
NP_001121189.2:p.Phe2024Ser
|
|
NM_001127718.4:c.1244T>C
|
NP_001121190.2:p.Phe415Ser
|
|
NM_198129.4:c.6239T>C
MANE Select
|
NP_937762.2:p.Phe2080Ser
|
|