ENST00000356141.9:c.2177C>A
MANE Select
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ENSP00000348460.4:p.Ala726Asp
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ENST00000551634.6:c.2186C>A
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ENSP00000448373.2:p.Ala729Asp
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|
ENST00000680362.1:c.2077C>A
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|
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ENST00000681323.1:c.793+2903C>A
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|
ENST00000346562.6:c.2081C>A
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ENSP00000319610.5:p.Ala694Asp
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ENST00000356141.8:c.2177C>A
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ENSP00000348460.4:p.Ala726Asp
|
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ENST00000357798.9:c.2138C>A
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ENSP00000350446.5:p.Ala713Asp
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ENST00000548645.5:c.2087C>A
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ENSP00000448916.1:p.Ala696Asp
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ENST00000551492.5:c.2192C>A
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ENSP00000450392.1:p.Ala731Asp
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ENST00000551634.5:c.2099C>A
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ENSP00000448373.1:p.Ala700Asp
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|
NM_001164749.1:c.2177C>A
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NP_001158221.1:p.Ala726Asp
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NM_001165893.1:c.2087C>A
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NP_001159365.1:p.Ala696Asp
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|
NM_022123.2:c.2081C>A
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NP_071406.1:p.Ala694Asp
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NM_173159.2:c.2138C>A
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NP_775182.1:p.Ala713Asp
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XM_005267991.2:c.2198C>A
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XP_005268048.1:p.Ala733Asp
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XM_005267992.2:c.2192C>A
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XP_005268049.1:p.Ala731Asp
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|
XM_005267993.2:c.2138C>A
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XP_005268050.1:p.Ala713Asp
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XM_011537067.1:c.2228C>A
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XP_011535369.1:p.Ala743Asp
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XM_011537068.1:c.2219C>A
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XP_011535370.1:p.Ala740Asp
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XM_011537069.1:c.2189C>A
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XP_011535371.1:p.Ala730Asp
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|
XM_011537070.1:c.2132C>A
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XP_011535372.1:p.Ala711Asp
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XM_011537071.1:c.2099C>A
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XP_011535373.1:p.Ala700Asp
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XM_011537072.1:c.2078C>A
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XP_011535374.1:p.Ala693Asp
|
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XM_011537073.1:c.1871C>A
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XP_011535375.1:p.Ala624Asp
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XM_011537074.1:c.1871C>A
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XP_011535376.1:p.Ala624Asp
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XM_005267991.3:c.2285C>A
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XP_005268048.2:p.Ala762Asp
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XM_005267992.3:c.2279C>A
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XP_005268049.2:p.Ala760Asp
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|
XM_011537067.2:c.2228C>A
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XP_011535369.1:p.Ala743Asp
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|
XM_011537069.2:c.2276C>A
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XP_011535371.2:p.Ala759Asp
|
|
XM_011537070.2:c.2132C>A
|
XP_011535372.1:p.Ala711Asp
|
|
XM_011537071.2:c.2186C>A
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XP_011535373.2:p.Ala729Asp
|
|
XM_011537072.2:c.2078C>A
|
XP_011535374.1:p.Ala693Asp
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XM_017021582.1:c.2336C>A
|
XP_016877071.1:p.Ala779Asp
|
|
XM_017021583.1:c.2327C>A
|
XP_016877072.1:p.Ala776Asp
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XM_017021584.1:c.2246C>A
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XP_016877073.1:p.Ala749Asp
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XM_017021585.1:c.2195C>A
|
XP_016877074.1:p.Ala732Asp
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XM_017021586.1:c.1871C>A
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XP_016877075.1:p.Ala624Asp
|
|
XM_017021587.1:c.1871C>A
|
XP_016877076.1:p.Ala624Asp
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|
XM_017021588.1:c.1871C>A
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XP_016877077.1:p.Ala624Asp
|
|
NM_001164749.2:c.2177C>A
MANE Select
|
NP_001158221.1:p.Ala726Asp
|
|
NM_001165893.2:c.2087C>A
|
NP_001159365.1:p.Ala696Asp
|
|
NM_022123.3:c.2081C>A
|
NP_071406.1:p.Ala694Asp
|
|
NM_173159.3:c.2138C>A
|
NP_775182.1:p.Ala713Asp
|
|
NM_001394988.1:c.2132C>A
|
NP_001381917.1:p.Ala711Asp
|
|
NM_001394989.1:c.2078C>A
|
NP_001381918.1:p.Ala693Asp
|
|