ENST00000209873.9:c.1081C>A
MANE Select
|
ENSP00000209873.4:p.Arg361Ser
|
|
ENST00000546562.6:n.2145C>A
|
|
|
ENST00000547238.6:n.1717C>A
|
|
|
ENST00000547520.6:n.1075C>A
|
|
|
ENST00000547757.2:c.130C>A
|
ENSP00000448020.2:p.Arg44Ser
|
|
ENST00000548880.2:n.1531C>A
|
|
|
ENST00000548931.6:c.601C>A
|
ENSP00000457518.1:p.Arg201Ser
|
|
ENST00000549450.6:n.1015C>A
|
|
|
ENST00000552161.6:n.2037C>A
|
|
|
ENST00000672797.1:n.1570C>A
|
|
|
ENST00000672900.1:n.2023C>A
|
|
|
ENST00000209873.8:c.1081C>A
|
ENSP00000209873.4:p.Arg361Ser
|
|
ENST00000394384.7:c.982C>A
|
ENSP00000377908.3:p.Arg328Ser
|
|
ENST00000548931.5:c.601C>A
|
ENSP00000457518.1:p.Arg201Ser
|
|
ENST00000550033.5:n.336C>A
|
|
|
ENST00000550286.5:c.709C>A
|
ENSP00000446885.1:p.Arg237Ser
|
|
ENST00000552876.5:n.1424C>A
|
|
|
NM_001173466.1:c.982C>A
|
NP_001166937.1:p.Arg328Ser
|
|
NM_015665.5:c.1081C>A
|
NP_056480.1:p.Arg361Ser
|
|
XM_006719617.2:c.1096C>A
|
XP_006719680.1:p.Arg366Ser
|
|
XM_011538777.1:c.1096C>A
|
XP_011537079.1:p.Arg366Ser
|
|
XM_011538778.1:c.1081C>A
|
XP_011537080.1:p.Arg361Ser
|
|
XM_011538779.1:c.997C>A
|
XP_011537081.1:p.Arg333Ser
|
|
XM_011538780.1:c.982C>A
|
XP_011537082.1:p.Arg328Ser
|
|
XM_011538781.1:c.430C>A
|
XP_011537083.1:p.Arg144Ser
|
|
XM_011538778.2:c.1081C>A
|
XP_011537080.1:p.Arg361Ser
|
|
XM_011538780.2:c.982C>A
|
XP_011537082.1:p.Arg328Ser
|
|
XR_001748875.2:n.1138C>A
|
|
|
NM_015665.6:c.1081C>A
MANE Select
|
NP_056480.1:p.Arg361Ser
|
|
NM_001173466.2:c.982C>A
|
NP_001166937.1:p.Arg328Ser
|
|