ENST00000270357.10:c.1583G>T
MANE Select
|
ENSP00000270357.4:p.Ser528Ile
|
|
ENST00000270357.8:c.890G>T
|
ENSP00000270357.3:p.Ser297Ile
|
|
ENST00000437406.1:c.149G>T
|
ENSP00000403319.1:p.Ser50Ile
|
|
ENST00000451363.5:c.224G>T
|
ENSP00000414661.1:p.Ser75Ile
|
|
ENST00000464550.5:n.419G>T
|
|
|
ENST00000471657.1:n.386G>T
|
|
|
ENST00000481757.5:n.2517G>T
|
|
|
ENST00000486058.5:n.1696G>T
|
|
|
ENST00000493398.5:n.729G>T
|
|
|
NM_018226.4:c.1583G>T
|
NP_060696.4:p.Ser528Ile
|
|
XM_005247036.3:c.1550G>T
|
XP_005247093.1:p.Ser517Ile
|
|
NM_018226.5:c.1583G>T
|
NP_060696.4:p.Ser528Ile
|
|
XM_005247036.4:c.1550G>T
|
XP_005247093.1:p.Ser517Ile
|
|
NM_018226.6:c.1583G>T
MANE Select
|
NP_060696.4:p.Ser528Ile
|
|