ENST00000270357.10:c.1580C>T
MANE Select
|
ENSP00000270357.4:p.Ser527Phe
|
|
ENST00000270357.8:c.887C>T
|
ENSP00000270357.3:p.Ser296Phe
|
|
ENST00000437406.1:c.146C>T
|
ENSP00000403319.1:p.Ser49Phe
|
|
ENST00000451363.5:c.221C>T
|
ENSP00000414661.1:p.Ser74Phe
|
|
ENST00000464550.5:n.416C>T
|
|
|
ENST00000471657.1:n.383C>T
|
|
|
ENST00000481757.5:n.2514C>T
|
|
|
ENST00000486058.5:n.1693C>T
|
|
|
ENST00000493398.5:n.726C>T
|
|
|
NM_018226.4:c.1580C>T
|
NP_060696.4:p.Ser527Phe
|
|
XM_005247036.3:c.1547C>T
|
XP_005247093.1:p.Ser516Phe
|
|
NM_018226.5:c.1580C>T
|
NP_060696.4:p.Ser527Phe
|
|
XM_005247036.4:c.1547C>T
|
XP_005247093.1:p.Ser516Phe
|
|
NM_018226.6:c.1580C>T
MANE Select
|
NP_060696.4:p.Ser527Phe
|
|