ENST00000270357.10:c.1583G>C
MANE Select
|
ENSP00000270357.4:p.Ser528Thr
|
|
ENST00000270357.8:c.890G>C
|
ENSP00000270357.3:p.Ser297Thr
|
|
ENST00000437406.1:c.149G>C
|
ENSP00000403319.1:p.Ser50Thr
|
|
ENST00000451363.5:c.224G>C
|
ENSP00000414661.1:p.Ser75Thr
|
|
ENST00000464550.5:n.419G>C
|
|
|
ENST00000471657.1:n.386G>C
|
|
|
ENST00000481757.5:n.2517G>C
|
|
|
ENST00000486058.5:n.1696G>C
|
|
|
ENST00000493398.5:n.729G>C
|
|
|
NM_018226.4:c.1583G>C
|
NP_060696.4:p.Ser528Thr
|
|
XM_005247036.3:c.1550G>C
|
XP_005247093.1:p.Ser517Thr
|
|
NM_018226.5:c.1583G>C
|
NP_060696.4:p.Ser528Thr
|
|
XM_005247036.4:c.1550G>C
|
XP_005247093.1:p.Ser517Thr
|
|
NM_018226.6:c.1583G>C
MANE Select
|
NP_060696.4:p.Ser528Thr
|
|