ENST00000466474.6:c.*1468A>C
|
ENSP00000511987.1:n.*1468A>C
|
|
ENST00000695525.1:n.3058A>C
|
|
|
ENST00000695558.1:c.2972A>C
|
ENSP00000512015.1:p.Glu991Ala
|
|
ENST00000703224.1:c.*2215A>C
|
ENSP00000515242.1:n.*2215A>C
|
|
ENST00000359568.10:c.2972A>C
MANE Select
|
ENSP00000352572.5:p.Glu991Ala
|
|
ENST00000359568.9:c.2972A>C
|
ENSP00000352572.5:p.Glu991Ala
|
|
ENST00000480896.5:n.3241A>C
|
|
|
NM_001315529.1:c.2618A>C
|
NP_001302458.1:p.Glu873Ala
|
|
NM_006031.5:c.2972A>C
|
NP_006022.3:p.Glu991Ala
|
|
XM_005261124.3:c.2972A>C
|
XP_005261181.1:p.Glu991Ala
|
|
XM_011529593.1:c.3053A>C
|
XP_011527895.1:p.Glu1018Ala
|
|
XM_011529594.1:c.3053A>C
|
XP_011527896.1:p.Glu1018Ala
|
|
XM_005261124.5:c.2972A>C
|
XP_005261181.1:p.Glu991Ala
|
|
XM_011529594.3:c.3053A>C
|
XP_011527896.1:p.Glu1018Ala
|
|
XM_017028362.2:c.2972A>C
|
XP_016883851.1:p.Glu991Ala
|
|
XM_017028363.1:c.2618A>C
|
XP_016883852.1:p.Glu873Ala
|
|
XM_024452082.1:c.1856A>C
|
XP_024307850.1:p.Glu619Ala
|
|
XM_024452083.1:c.752A>C
|
XP_024307851.1:p.Glu251Ala
|
|
NM_006031.6:c.2972A>C
MANE Select
|
NP_006022.3:p.Glu991Ala
|
|
NM_001315529.2:c.2618A>C
|
NP_001302458.1:p.Glu873Ala
|
|