ENST00000370263.9:c.793T=
MANE Select
|
ENSP00000359285.4:p.Phe265=
|
|
ENST00000370263.8:c.793T=
|
ENSP00000359285.4:p.Phe265=
|
|
ENST00000463705.5:n.1441T=
|
|
|
ENST00000467563.3:n.863T=
|
|
|
ENST00000498043.6:c.817T=
|
|
|
ENST00000615287.4:c.580T=
|
ENSP00000483388.1:p.Phe194=
|
|
ENST00000627000.1:c.*482T=
|
ENSP00000486914.1:n.*482T=
|
|
ENST00000630240.1:n.514T=
|
|
|
NM_000744.6:c.793T=
|
NP_000735.1:p.Phe265=
|
|
NM_001256573.1:c.265T=
|
NP_001243502.1:p.Phe89=
|
|
NR_046317.1:n.1049T=
|
|
|
XM_011528524.1:c.580T=
|
XP_011526826.1:p.Phe194=
|
|
XM_017027625.2:c.265T=
|
XP_016883114.1:p.Phe89=
|
|
XM_024451822.1:c.265T=
|
XP_024307590.1:p.Phe89=
|
|
NM_001256573.2:c.265T=
|
NP_001243502.1:p.Phe89=
|
|
NR_046317.2:n.1002T=
|
|
|
NM_000744.7:c.793T=
MANE Select
|
NP_000735.1:p.Phe265=
|
|