ENST00000246337.9:c.1004C>T
MANE Select
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ENSP00000246337.4:p.Ala335Val
|
|
ENST00000491773.6:c.761C>T
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ENSP00000498551.1:p.Ala254Val
|
|
ENST00000636293.1:c.866C>T
|
ENSP00000490710.1:p.Ala289Val
|
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ENST00000636836.1:c.*40C>T
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ENSP00000490594.1:n.*40C>T
|
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ENST00000651476.1:c.899C>T
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ENSP00000498668.1:p.Ala300Val
|
|
ENST00000652165.1:c.761C>T
|
ENSP00000498295.1:p.Ala254Val
|
|
ENST00000652287.1:c.941C>T
|
ENSP00000498413.1:p.Ala314Val
|
|
ENST00000652514.1:c.965C>T
|
ENSP00000498635.1:n.965C>T
|
|
ENST00000246337.8:c.1004C>T
|
ENSP00000246337.4:p.Ala335Val
|
|
ENST00000465678.1:n.749C>T
|
|
|
ENST00000472254.1:n.757C>T
|
|
|
ENST00000494399.5:n.1671C>T
|
|
|
NM_000374.4:c.1004C>T
|
NP_000365.3:p.Ala335Val
|
|
NR_036510.1:n.1187C>T
|
|
|
XM_005271169.1:c.788C>T
|
XP_005271226.1:p.Ala263Val
|
|
XM_005271170.1:c.788C>T
|
XP_005271227.1:p.Ala263Val
|
|
XM_011542080.1:c.941C>T
|
XP_011540382.1:p.Ala314Val
|
|
XM_011542081.1:c.836C>T
|
XP_011540383.1:p.Ala279Val
|
|
NM_000374.5:c.1004C>T
MANE Select
|
NP_000365.3:p.Ala335Val
|
|
NR_158184.1:n.1085C>T
|
|
|
NR_158185.1:n.1035C>T
|
|
|
NR_036510.2:n.1066C>T
|
|
|