ENST00000209873.9:c.1528G>C
MANE Select
|
ENSP00000209873.4:p.Gly510Arg
|
|
ENST00000546562.6:n.2592G>C
|
|
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ENST00000547238.6:n.2164G>C
|
|
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ENST00000547520.6:n.1644G>C
|
|
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ENST00000547757.2:c.*446G>C
|
ENSP00000448020.2:n.*446G>C
|
|
ENST00000548931.6:c.963G>C
|
ENSP00000457518.1:p.Glu321Asp
|
|
ENST00000549450.6:n.1462G>C
|
|
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ENST00000672797.1:n.2017G>C
|
|
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ENST00000209873.8:c.1528G>C
|
ENSP00000209873.4:p.Gly510Arg
|
|
ENST00000394384.7:c.1429G>C
|
ENSP00000377908.3:p.Gly477Arg
|
|
ENST00000548931.5:c.963G>C
|
ENSP00000457518.1:p.Glu321Asp
|
|
ENST00000550286.5:c.1156G>C
|
ENSP00000446885.1:p.Gly386Arg
|
|
ENST00000552876.5:n.1871G>C
|
|
|
NM_001173466.1:c.1429G>C
|
NP_001166937.1:p.Gly477Arg
|
|
NM_015665.5:c.1528G>C
|
NP_056480.1:p.Gly510Arg
|
|
XM_006719617.2:c.1543G>C
|
XP_006719680.1:p.Gly515Arg
|
|
XM_011538777.1:c.1585G>C
|
XP_011537079.1:p.Gly529Arg
|
|
XM_011538778.1:c.1570G>C
|
XP_011537080.1:p.Gly524Arg
|
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XM_011538779.1:c.1486G>C
|
XP_011537081.1:p.Gly496Arg
|
|
XM_011538780.1:c.1471G>C
|
XP_011537082.1:p.Gly491Arg
|
|
XM_011538781.1:c.919G>C
|
XP_011537083.1:p.Gly307Arg
|
|
XM_011538778.2:c.1570G>C
|
XP_011537080.1:p.Gly524Arg
|
|
XM_011538780.2:c.1471G>C
|
XP_011537082.1:p.Gly491Arg
|
|
XR_001748875.2:n.1585G>C
|
|
|
NM_015665.6:c.1528G>C
MANE Select
|
NP_056480.1:p.Gly510Arg
|
|
NM_001173466.2:c.1429G>C
|
NP_001166937.1:p.Gly477Arg
|
|