ENST00000356141.9:c.2220C>A
MANE Select
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ENSP00000348460.4:p.Ala740=
|
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ENST00000551634.6:c.2229C>A
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ENSP00000448373.2:p.Ala743=
|
|
ENST00000680362.1:c.2120C>A
|
|
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ENST00000681323.1:c.793+2946C>A
|
|
|
ENST00000346562.6:c.2124C>A
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ENSP00000319610.5:p.Ala708=
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|
ENST00000356141.8:c.2220C>A
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ENSP00000348460.4:p.Ala740=
|
|
ENST00000357798.9:c.2181C>A
|
ENSP00000350446.5:p.Ala727=
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|
ENST00000548645.5:c.2130C>A
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ENSP00000448916.1:p.Ala710=
|
|
ENST00000551492.5:c.2235C>A
|
ENSP00000450392.1:p.Ala745=
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ENST00000551634.5:c.2142C>A
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ENSP00000448373.1:p.Ala714=
|
|
NM_001164749.1:c.2220C>A
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NP_001158221.1:p.Ala740=
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|
NM_001165893.1:c.2130C>A
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NP_001159365.1:p.Ala710=
|
|
NM_022123.2:c.2124C>A
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NP_071406.1:p.Ala708=
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NM_173159.2:c.2181C>A
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NP_775182.1:p.Ala727=
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|
XM_005267991.2:c.2241C>A
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XP_005268048.1:p.Ala747=
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XM_005267992.2:c.2235C>A
|
XP_005268049.1:p.Ala745=
|
|
XM_005267993.2:c.2181C>A
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XP_005268050.1:p.Ala727=
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|
XM_011537067.1:c.2271C>A
|
XP_011535369.1:p.Ala757=
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|
XM_011537068.1:c.2262C>A
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XP_011535370.1:p.Ala754=
|
|
XM_011537069.1:c.2232C>A
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XP_011535371.1:p.Ala744=
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|
XM_011537070.1:c.2175C>A
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XP_011535372.1:p.Ala725=
|
|
XM_011537071.1:c.2142C>A
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XP_011535373.1:p.Ala714=
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|
XM_011537072.1:c.2121C>A
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XP_011535374.1:p.Ala707=
|
|
XM_011537073.1:c.1914C>A
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XP_011535375.1:p.Ala638=
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|
XM_011537074.1:c.1914C>A
|
XP_011535376.1:p.Ala638=
|
|
XM_005267991.3:c.2328C>A
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XP_005268048.2:p.Ala776=
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|
XM_005267992.3:c.2322C>A
|
XP_005268049.2:p.Ala774=
|
|
XM_011537067.2:c.2271C>A
|
XP_011535369.1:p.Ala757=
|
|
XM_011537069.2:c.2319C>A
|
XP_011535371.2:p.Ala773=
|
|
XM_011537070.2:c.2175C>A
|
XP_011535372.1:p.Ala725=
|
|
XM_011537071.2:c.2229C>A
|
XP_011535373.2:p.Ala743=
|
|
XM_011537072.2:c.2121C>A
|
XP_011535374.1:p.Ala707=
|
|
XM_017021582.1:c.2379C>A
|
XP_016877071.1:p.Ala793=
|
|
XM_017021583.1:c.2370C>A
|
XP_016877072.1:p.Ala790=
|
|
XM_017021584.1:c.2289C>A
|
XP_016877073.1:p.Ala763=
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|
XM_017021585.1:c.2238C>A
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XP_016877074.1:p.Ala746=
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|
XM_017021586.1:c.1914C>A
|
XP_016877075.1:p.Ala638=
|
|
XM_017021587.1:c.1914C>A
|
XP_016877076.1:p.Ala638=
|
|
XM_017021588.1:c.1914C>A
|
XP_016877077.1:p.Ala638=
|
|
NM_001164749.2:c.2220C>A
MANE Select
|
NP_001158221.1:p.Ala740=
|
|
NM_001165893.2:c.2130C>A
|
NP_001159365.1:p.Ala710=
|
|
NM_022123.3:c.2124C>A
|
NP_071406.1:p.Ala708=
|
|
NM_173159.3:c.2181C>A
|
NP_775182.1:p.Ala727=
|
|
NM_001394988.1:c.2175C>A
|
NP_001381917.1:p.Ala725=
|
|
NM_001394989.1:c.2121C>A
|
NP_001381918.1:p.Ala707=
|
|