ENST00000209873.9:c.1085G>C
MANE Select
|
ENSP00000209873.4:p.Cys362Ser
|
|
ENST00000546562.6:n.2149G>C
|
|
|
ENST00000547238.6:n.1721G>C
|
|
|
ENST00000547520.6:n.1079G>C
|
|
|
ENST00000547757.2:c.134G>C
|
ENSP00000448020.2:p.Cys45Ser
|
|
ENST00000548880.2:n.1535G>C
|
|
|
ENST00000548931.6:c.605G>C
|
ENSP00000457518.1:p.Cys202Ser
|
|
ENST00000549450.6:n.1019G>C
|
|
|
ENST00000552161.6:n.2041G>C
|
|
|
ENST00000672797.1:n.1574G>C
|
|
|
ENST00000672900.1:n.2027G>C
|
|
|
ENST00000209873.8:c.1085G>C
|
ENSP00000209873.4:p.Cys362Ser
|
|
ENST00000394384.7:c.986G>C
|
ENSP00000377908.3:p.Cys329Ser
|
|
ENST00000548931.5:c.605G>C
|
ENSP00000457518.1:p.Cys202Ser
|
|
ENST00000550033.5:n.340G>C
|
|
|
ENST00000550286.5:c.713G>C
|
ENSP00000446885.1:p.Cys238Ser
|
|
ENST00000552876.5:n.1428G>C
|
|
|
NM_001173466.1:c.986G>C
|
NP_001166937.1:p.Cys329Ser
|
|
NM_015665.5:c.1085G>C
|
NP_056480.1:p.Cys362Ser
|
|
XM_006719617.2:c.1100G>C
|
XP_006719680.1:p.Cys367Ser
|
|
XM_011538777.1:c.1100G>C
|
XP_011537079.1:p.Cys367Ser
|
|
XM_011538778.1:c.1085G>C
|
XP_011537080.1:p.Cys362Ser
|
|
XM_011538779.1:c.1001G>C
|
XP_011537081.1:p.Cys334Ser
|
|
XM_011538780.1:c.986G>C
|
XP_011537082.1:p.Cys329Ser
|
|
XM_011538781.1:c.434G>C
|
XP_011537083.1:p.Cys145Ser
|
|
XM_011538778.2:c.1085G>C
|
XP_011537080.1:p.Cys362Ser
|
|
XM_011538780.2:c.986G>C
|
XP_011537082.1:p.Cys329Ser
|
|
XR_001748875.2:n.1142G>C
|
|
|
NM_015665.6:c.1085G>C
MANE Select
|
NP_056480.1:p.Cys362Ser
|
|
NM_001173466.2:c.986G>C
|
NP_001166937.1:p.Cys329Ser
|
|