ENST00000209873.9:c.1558G>C
MANE Select
|
ENSP00000209873.4:p.Glu520Gln
|
|
ENST00000546562.6:n.2622G>C
|
|
|
ENST00000547238.6:n.2194G>C
|
|
|
ENST00000547520.6:n.1674G>C
|
|
|
ENST00000547757.2:c.*476G>C
|
ENSP00000448020.2:n.*476G>C
|
|
ENST00000548931.6:c.993G>C
|
ENSP00000457518.1:p.Leu331=
|
|
ENST00000549450.6:n.1492G>C
|
|
|
ENST00000672797.1:n.2047G>C
|
|
|
ENST00000209873.8:c.1558G>C
|
ENSP00000209873.4:p.Glu520Gln
|
|
ENST00000394384.7:c.1459G>C
|
ENSP00000377908.3:p.Glu487Gln
|
|
ENST00000548931.5:c.993G>C
|
ENSP00000457518.1:p.Leu331=
|
|
ENST00000550286.5:c.1186G>C
|
ENSP00000446885.1:p.Glu396Gln
|
|
ENST00000552876.5:n.1901G>C
|
|
|
NM_001173466.1:c.1459G>C
|
NP_001166937.1:p.Glu487Gln
|
|
NM_015665.5:c.1558G>C
|
NP_056480.1:p.Glu520Gln
|
|
XM_006719617.2:c.1573G>C
|
XP_006719680.1:p.Glu525Gln
|
|
XM_011538777.1:c.1615G>C
|
XP_011537079.1:p.Glu539Gln
|
|
XM_011538778.1:c.1600G>C
|
XP_011537080.1:p.Glu534Gln
|
|
XM_011538779.1:c.1516G>C
|
XP_011537081.1:p.Glu506Gln
|
|
XM_011538780.1:c.1501G>C
|
XP_011537082.1:p.Glu501Gln
|
|
XM_011538781.1:c.949G>C
|
XP_011537083.1:p.Glu317Gln
|
|
XM_011538778.2:c.1600G>C
|
XP_011537080.1:p.Glu534Gln
|
|
XM_011538780.2:c.1501G>C
|
XP_011537082.1:p.Glu501Gln
|
|
XR_001748875.2:n.1615G>C
|
|
|
NM_015665.6:c.1558G>C
MANE Select
|
NP_056480.1:p.Glu520Gln
|
|
NM_001173466.2:c.1459G>C
|
NP_001166937.1:p.Glu487Gln
|
|