ENST00000366577.10:c.1806A>T
MANE Select
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ENSP00000355536.5:p.Ala602=
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ENST00000535889.6:c.1806A>T
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ENSP00000441845.1:p.Ala602=
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|
ENST00000650888.1:c.*848A>T
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ENSP00000498393.1:n.*848A>T
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ENST00000651455.1:c.*550A>T
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ENSP00000498963.1:n.*550A>T
|
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ENST00000674797.2:c.1458A>T
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ENSP00000502299.2:p.Ala486=
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ENST00000679569.1:n.2120A>T
|
|
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ENST00000679842.1:c.1806A>T
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ENSP00000506109.1:p.Ala602=
|
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ENST00000680454.1:n.2250A>T
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|
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ENST00000681102.1:c.1626A>T
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ENSP00000505600.1:p.Ala542=
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ENST00000681177.1:c.1516-7202A>T
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ENSP00000506327.1:n.1516-7202A>T
|
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ENST00000681937.1:n.2148-7202A>T
|
|
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ENST00000366576.3:c.468A>T
|
ENSP00000355535.3:p.Ala156=
|
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ENST00000366577.9:c.1806A>T
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ENSP00000355536.5:p.Ala602=
|
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ENST00000463959.1:n.1825A>T
|
|
|
ENST00000535889.5:c.1806A>T
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ENSP00000441845.1:p.Ala602=
|
|
NM_000254.2:c.1806A>T
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NP_000245.2:p.Ala602=
|
|
NM_001291939.1:c.1806A>T
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NP_001278868.1:p.Ala602=
|
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NM_001291940.1:c.585A>T
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NP_001278869.1:p.Ala195=
|
|
XM_005273141.3:c.1803A>T
|
XP_005273198.1:p.Ala601=
|
|
XM_006711769.2:c.1806A>T
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XP_006711832.1:p.Ala602=
|
|
XM_006711770.1:c.870A>T
|
XP_006711833.1:p.Ala290=
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|
XM_011544193.1:c.1806A>T
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XP_011542495.1:p.Ala602=
|
|
XM_011544194.1:c.1974A>T
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XP_011542496.1:p.Ala658=
|
|
XM_005273141.5:c.1803A>T
|
XP_005273198.1:p.Ala601=
|
|
XM_006711770.3:c.870A>T
|
XP_006711833.1:p.Ala290=
|
|
XM_011544194.3:c.1974A>T
|
XP_011542496.1:p.Ala658=
|
|
XM_017001329.2:c.1974A>T
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XP_016856818.1:p.Ala658=
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|
XM_017001330.2:c.1974A>T
|
XP_016856819.1:p.Ala658=
|
|
NM_001291940.2:c.585A>T
|
NP_001278869.1:p.Ala195=
|
|
NM_000254.3:c.1806A>T
MANE Select
|
NP_000245.2:p.Ala602=
|
|