ENST00000370263.9:c.499T>G
MANE Select
|
ENSP00000359285.4:p.Phe167Val
|
|
ENST00000370263.8:c.499T>G
|
ENSP00000359285.4:p.Phe167Val
|
|
ENST00000463705.5:n.1147T>G
|
|
|
ENST00000467563.3:n.569T>G
|
|
|
ENST00000498043.6:c.523T>G
|
|
|
ENST00000615287.4:c.286T>G
|
ENSP00000483388.1:p.Phe96Val
|
|
ENST00000627000.1:c.*188T>G
|
ENSP00000486914.1:n.*188T>G
|
|
ENST00000628665.1:n.542T>G
|
|
|
ENST00000630240.1:n.220T>G
|
|
|
NM_000744.6:c.499T>G
|
NP_000735.1:p.Phe167Val
|
|
NM_001256573.1:c.-30T>G
|
NP_001243502.1:n.-30T>G
|
|
NR_046317.1:n.755T>G
|
|
|
XM_011528524.1:c.286T>G
|
XP_011526826.1:p.Phe96Val
|
|
XM_017027625.2:c.-30T>G
|
XP_016883114.1:n.-30T>G
|
|
XM_024451822.1:c.-30T>G
|
XP_024307590.1:n.-30T>G
|
|
NM_001256573.2:c.-30T>G
|
NP_001243502.1:n.-30T>G
|
|
NR_046317.2:n.708T>G
|
|
|
NM_000744.7:c.499T>G
MANE Select
|
NP_000735.1:p.Phe167Val
|
|