ENST00000268695.10:c.844T>G
MANE Select
|
ENSP00000268695.5:p.Phe282Val
|
|
ENST00000268695.9:c.844T>G
|
ENSP00000268695.5:p.Phe282Val
|
|
ENST00000562593.5:n.4253T>G
|
|
|
ENST00000562931.5:n.432T>G
|
|
|
ENST00000567525.5:c.525T>G
|
ENSP00000454484.1:n.525T>G
|
|
ENST00000568613.5:c.963T>G
|
ENSP00000457921.1:n.963T>G
|
|
NM_000512.4:c.844T>G
|
NP_000503.1:p.Phe282Val
|
|
XM_005256301.2:c.844T>G
|
XP_005256358.1:p.Phe282Val
|
|
XM_005256302.1:c.862T>G
|
XP_005256359.1:p.Phe288Val
|
|
XM_011522982.1:c.862T>G
|
XP_011521284.1:p.Phe288Val
|
|
XM_011522984.1:c.862T>G
|
XP_011521286.1:p.Phe288Val
|
|
NM_001323543.1:c.289T>G
|
NP_001310472.1:p.Phe97Val
|
|
NM_001323544.1:c.862T>G
|
NP_001310473.1:p.Phe288Val
|
|
XM_005256301.3:c.844T>G
|
XP_005256358.1:p.Phe282Val
|
|
XM_011522982.2:c.862T>G
|
XP_011521284.1:p.Phe288Val
|
|
XM_017023111.2:c.862T>G
|
XP_016878600.1:p.Phe288Val
|
|
XM_017023112.2:c.862T>G
|
XP_016878601.1:p.Phe288Val
|
|
XM_017023113.1:c.289T>G
|
XP_016878602.1:p.Phe97Val
|
|
NM_000512.5:c.844T>G
MANE Select
|
NP_000503.1:p.Phe282Val
|
|
NM_001323543.2:c.289T>G
|
NP_001310472.1:p.Phe97Val
|
|
NM_001323544.2:c.862T>G
|
NP_001310473.1:p.Phe288Val
|
|