ENST00000209873.9:c.1598G>T
MANE Select
|
ENSP00000209873.4:p.Gly533Val
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ENST00000546562.6:n.2662G>T
|
|
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ENST00000547238.6:n.2234G>T
|
|
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ENST00000547757.2:c.*516G>T
|
ENSP00000448020.2:n.*516G>T
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ENST00000548931.6:c.1033G>T
|
ENSP00000457518.1:p.Gly345Cys
|
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ENST00000549450.6:n.1532G>T
|
|
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ENST00000672797.1:n.2087G>T
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ENST00000209873.8:c.1598G>T
|
ENSP00000209873.4:p.Gly533Val
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|
ENST00000394384.7:c.1499G>T
|
ENSP00000377908.3:p.Gly500Val
|
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ENST00000548931.5:c.1033G>T
|
ENSP00000457518.1:p.Gly345Cys
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ENST00000550286.5:c.1226G>T
|
ENSP00000446885.1:p.Gly409Val
|
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ENST00000552876.5:n.1941G>T
|
|
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NM_001173466.1:c.1499G>T
|
NP_001166937.1:p.Gly500Val
|
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NM_015665.5:c.1598G>T
|
NP_056480.1:p.Gly533Val
|
|
XM_006719617.2:c.1613G>T
|
XP_006719680.1:p.Gly538Val
|
|
XM_011538777.1:c.1655G>T
|
XP_011537079.1:p.Gly552Val
|
|
XM_011538778.1:c.1640G>T
|
XP_011537080.1:p.Gly547Val
|
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XM_011538779.1:c.1556G>T
|
XP_011537081.1:p.Gly519Val
|
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XM_011538780.1:c.1541G>T
|
XP_011537082.1:p.Gly514Val
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XM_011538781.1:c.989G>T
|
XP_011537083.1:p.Gly330Val
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XM_011538778.2:c.1640G>T
|
XP_011537080.1:p.Gly547Val
|
|
XM_011538780.2:c.1541G>T
|
XP_011537082.1:p.Gly514Val
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XR_001748875.2:n.1655G>T
|
|
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NM_015665.6:c.1598G>T
MANE Select
|
NP_056480.1:p.Gly533Val
|
|
NM_001173466.2:c.1499G>T
|
NP_001166937.1:p.Gly500Val
|
|