ENST00000356141.9:c.2214C>A
MANE Select
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ENSP00000348460.4:p.Ala738=
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ENST00000551634.6:c.2223C>A
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ENSP00000448373.2:p.Ala741=
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ENST00000680362.1:c.2114C>A
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|
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ENST00000681323.1:c.793+2940C>A
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|
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ENST00000346562.6:c.2118C>A
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ENSP00000319610.5:p.Ala706=
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ENST00000356141.8:c.2214C>A
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ENSP00000348460.4:p.Ala738=
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ENST00000357798.9:c.2175C>A
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ENSP00000350446.5:p.Ala725=
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ENST00000548645.5:c.2124C>A
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ENSP00000448916.1:p.Ala708=
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ENST00000551492.5:c.2229C>A
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ENSP00000450392.1:p.Ala743=
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ENST00000551634.5:c.2136C>A
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ENSP00000448373.1:p.Ala712=
|
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NM_001164749.1:c.2214C>A
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NP_001158221.1:p.Ala738=
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NM_001165893.1:c.2124C>A
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NP_001159365.1:p.Ala708=
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NM_022123.2:c.2118C>A
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NP_071406.1:p.Ala706=
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NM_173159.2:c.2175C>A
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NP_775182.1:p.Ala725=
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|
XM_005267991.2:c.2235C>A
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XP_005268048.1:p.Ala745=
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XM_005267992.2:c.2229C>A
|
XP_005268049.1:p.Ala743=
|
|
XM_005267993.2:c.2175C>A
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XP_005268050.1:p.Ala725=
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XM_011537067.1:c.2265C>A
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XP_011535369.1:p.Ala755=
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XM_011537068.1:c.2256C>A
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XP_011535370.1:p.Ala752=
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XM_011537069.1:c.2226C>A
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XP_011535371.1:p.Ala742=
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XM_011537070.1:c.2169C>A
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XP_011535372.1:p.Ala723=
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XM_011537071.1:c.2136C>A
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XP_011535373.1:p.Ala712=
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XM_011537072.1:c.2115C>A
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XP_011535374.1:p.Ala705=
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|
XM_011537073.1:c.1908C>A
|
XP_011535375.1:p.Ala636=
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|
XM_011537074.1:c.1908C>A
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XP_011535376.1:p.Ala636=
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|
XM_005267991.3:c.2322C>A
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XP_005268048.2:p.Ala774=
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XM_005267992.3:c.2316C>A
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XP_005268049.2:p.Ala772=
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|
XM_011537067.2:c.2265C>A
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XP_011535369.1:p.Ala755=
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|
XM_011537069.2:c.2313C>A
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XP_011535371.2:p.Ala771=
|
|
XM_011537070.2:c.2169C>A
|
XP_011535372.1:p.Ala723=
|
|
XM_011537071.2:c.2223C>A
|
XP_011535373.2:p.Ala741=
|
|
XM_011537072.2:c.2115C>A
|
XP_011535374.1:p.Ala705=
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|
XM_017021582.1:c.2373C>A
|
XP_016877071.1:p.Ala791=
|
|
XM_017021583.1:c.2364C>A
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XP_016877072.1:p.Ala788=
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XM_017021584.1:c.2283C>A
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XP_016877073.1:p.Ala761=
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XM_017021585.1:c.2232C>A
|
XP_016877074.1:p.Ala744=
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|
XM_017021586.1:c.1908C>A
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XP_016877075.1:p.Ala636=
|
|
XM_017021587.1:c.1908C>A
|
XP_016877076.1:p.Ala636=
|
|
XM_017021588.1:c.1908C>A
|
XP_016877077.1:p.Ala636=
|
|
NM_001164749.2:c.2214C>A
MANE Select
|
NP_001158221.1:p.Ala738=
|
|
NM_001165893.2:c.2124C>A
|
NP_001159365.1:p.Ala708=
|
|
NM_022123.3:c.2118C>A
|
NP_071406.1:p.Ala706=
|
|
NM_173159.3:c.2175C>A
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NP_775182.1:p.Ala725=
|
|
NM_001394988.1:c.2169C>A
|
NP_001381917.1:p.Ala723=
|
|
NM_001394989.1:c.2115C>A
|
NP_001381918.1:p.Ala705=
|
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