ENST00000356141.9:c.2110G>T
MANE Select
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ENSP00000348460.4:p.Gly704Cys
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ENST00000551634.6:c.2119G>T
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ENSP00000448373.2:p.Gly707Cys
|
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ENST00000680362.1:c.2010G>T
|
|
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ENST00000681323.1:c.793+2836G>T
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ENST00000346562.6:c.2014G>T
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ENSP00000319610.5:p.Gly672Cys
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ENST00000356141.8:c.2110G>T
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ENSP00000348460.4:p.Gly704Cys
|
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ENST00000357798.9:c.2071G>T
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ENSP00000350446.5:p.Gly691Cys
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ENST00000548645.5:c.2020G>T
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ENSP00000448916.1:p.Gly674Cys
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ENST00000551492.5:c.2125G>T
|
ENSP00000450392.1:p.Gly709Cys
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ENST00000551634.5:c.2032G>T
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ENSP00000448373.1:p.Gly678Cys
|
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NM_001164749.1:c.2110G>T
|
NP_001158221.1:p.Gly704Cys
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|
NM_001165893.1:c.2020G>T
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NP_001159365.1:p.Gly674Cys
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|
NM_022123.2:c.2014G>T
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NP_071406.1:p.Gly672Cys
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NM_173159.2:c.2071G>T
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NP_775182.1:p.Gly691Cys
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|
XM_005267991.2:c.2131G>T
|
XP_005268048.1:p.Gly711Cys
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XM_005267992.2:c.2125G>T
|
XP_005268049.1:p.Gly709Cys
|
|
XM_005267993.2:c.2071G>T
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XP_005268050.1:p.Gly691Cys
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XM_011537067.1:c.2161G>T
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XP_011535369.1:p.Gly721Cys
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XM_011537068.1:c.2152G>T
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XP_011535370.1:p.Gly718Cys
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XM_011537069.1:c.2122G>T
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XP_011535371.1:p.Gly708Cys
|
|
XM_011537070.1:c.2065G>T
|
XP_011535372.1:p.Gly689Cys
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|
XM_011537071.1:c.2032G>T
|
XP_011535373.1:p.Gly678Cys
|
|
XM_011537072.1:c.2011G>T
|
XP_011535374.1:p.Gly671Cys
|
|
XM_011537073.1:c.1804G>T
|
XP_011535375.1:p.Gly602Cys
|
|
XM_011537074.1:c.1804G>T
|
XP_011535376.1:p.Gly602Cys
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XM_005267991.3:c.2218G>T
|
XP_005268048.2:p.Gly740Cys
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|
XM_005267992.3:c.2212G>T
|
XP_005268049.2:p.Gly738Cys
|
|
XM_011537067.2:c.2161G>T
|
XP_011535369.1:p.Gly721Cys
|
|
XM_011537069.2:c.2209G>T
|
XP_011535371.2:p.Gly737Cys
|
|
XM_011537070.2:c.2065G>T
|
XP_011535372.1:p.Gly689Cys
|
|
XM_011537071.2:c.2119G>T
|
XP_011535373.2:p.Gly707Cys
|
|
XM_011537072.2:c.2011G>T
|
XP_011535374.1:p.Gly671Cys
|
|
XM_017021582.1:c.2269G>T
|
XP_016877071.1:p.Gly757Cys
|
|
XM_017021583.1:c.2260G>T
|
XP_016877072.1:p.Gly754Cys
|
|
XM_017021584.1:c.2179G>T
|
XP_016877073.1:p.Gly727Cys
|
|
XM_017021585.1:c.2128G>T
|
XP_016877074.1:p.Gly710Cys
|
|
XM_017021586.1:c.1804G>T
|
XP_016877075.1:p.Gly602Cys
|
|
XM_017021587.1:c.1804G>T
|
XP_016877076.1:p.Gly602Cys
|
|
XM_017021588.1:c.1804G>T
|
XP_016877077.1:p.Gly602Cys
|
|
NM_001164749.2:c.2110G>T
MANE Select
|
NP_001158221.1:p.Gly704Cys
|
|
NM_001165893.2:c.2020G>T
|
NP_001159365.1:p.Gly674Cys
|
|
NM_022123.3:c.2014G>T
|
NP_071406.1:p.Gly672Cys
|
|
NM_173159.3:c.2071G>T
|
NP_775182.1:p.Gly691Cys
|
|
NM_001394988.1:c.2065G>T
|
NP_001381917.1:p.Gly689Cys
|
|
NM_001394989.1:c.2011G>T
|
NP_001381918.1:p.Gly671Cys
|
|