ENST00000356141.9:c.1817G>A
MANE Select
|
ENSP00000348460.4:p.Arg606Gln
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|
ENST00000551634.6:c.1826G>A
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ENSP00000448373.2:p.Arg609Gln
|
|
ENST00000680362.1:c.1717G>A
|
|
|
ENST00000681323.1:c.793+2543G>A
|
|
|
ENST00000346562.6:c.1721G>A
|
ENSP00000319610.5:p.Arg574Gln
|
|
ENST00000356141.8:c.1817G>A
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ENSP00000348460.4:p.Arg606Gln
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|
ENST00000357798.9:c.1778G>A
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ENSP00000350446.5:p.Arg593Gln
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|
ENST00000548645.5:c.1727G>A
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ENSP00000448916.1:p.Arg576Gln
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|
ENST00000551492.5:c.1832G>A
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ENSP00000450392.1:p.Arg611Gln
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|
ENST00000551634.5:c.1739G>A
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ENSP00000448373.1:p.Arg580Gln
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|
NM_001164749.1:c.1817G>A
|
NP_001158221.1:p.Arg606Gln
|
|
NM_001165893.1:c.1727G>A
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NP_001159365.1:p.Arg576Gln
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|
NM_022123.2:c.1721G>A
|
NP_071406.1:p.Arg574Gln
|
|
NM_173159.2:c.1778G>A
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NP_775182.1:p.Arg593Gln
|
|
XM_005267991.2:c.1838G>A
|
XP_005268048.1:p.Arg613Gln
|
|
XM_005267992.2:c.1832G>A
|
XP_005268049.1:p.Arg611Gln
|
|
XM_005267993.2:c.1778G>A
|
XP_005268050.1:p.Arg593Gln
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|
XM_011537067.1:c.1868G>A
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XP_011535369.1:p.Arg623Gln
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|
XM_011537068.1:c.1859G>A
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XP_011535370.1:p.Arg620Gln
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|
XM_011537069.1:c.1829G>A
|
XP_011535371.1:p.Arg610Gln
|
|
XM_011537070.1:c.1772G>A
|
XP_011535372.1:p.Arg591Gln
|
|
XM_011537071.1:c.1739G>A
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XP_011535373.1:p.Arg580Gln
|
|
XM_011537072.1:c.1718G>A
|
XP_011535374.1:p.Arg573Gln
|
|
XM_011537073.1:c.1511G>A
|
XP_011535375.1:p.Arg504Gln
|
|
XM_011537074.1:c.1511G>A
|
XP_011535376.1:p.Arg504Gln
|
|
XM_005267991.3:c.1925G>A
|
XP_005268048.2:p.Arg642Gln
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|
XM_005267992.3:c.1919G>A
|
XP_005268049.2:p.Arg640Gln
|
|
XM_011537067.2:c.1868G>A
|
XP_011535369.1:p.Arg623Gln
|
|
XM_011537069.2:c.1916G>A
|
XP_011535371.2:p.Arg639Gln
|
|
XM_011537070.2:c.1772G>A
|
XP_011535372.1:p.Arg591Gln
|
|
XM_011537071.2:c.1826G>A
|
XP_011535373.2:p.Arg609Gln
|
|
XM_011537072.2:c.1718G>A
|
XP_011535374.1:p.Arg573Gln
|
|
XM_017021582.1:c.1976G>A
|
XP_016877071.1:p.Arg659Gln
|
|
XM_017021583.1:c.1967G>A
|
XP_016877072.1:p.Arg656Gln
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|
XM_017021584.1:c.1886G>A
|
XP_016877073.1:p.Arg629Gln
|
|
XM_017021585.1:c.1835G>A
|
XP_016877074.1:p.Arg612Gln
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|
XM_017021586.1:c.1511G>A
|
XP_016877075.1:p.Arg504Gln
|
|
XM_017021587.1:c.1511G>A
|
XP_016877076.1:p.Arg504Gln
|
|
XM_017021588.1:c.1511G>A
|
XP_016877077.1:p.Arg504Gln
|
|
NM_001164749.2:c.1817G>A
MANE Select
|
NP_001158221.1:p.Arg606Gln
|
|
NM_001165893.2:c.1727G>A
|
NP_001159365.1:p.Arg576Gln
|
|
NM_022123.3:c.1721G>A
|
NP_071406.1:p.Arg574Gln
|
|
NM_173159.3:c.1778G>A
|
NP_775182.1:p.Arg593Gln
|
|
NM_001394988.1:c.1772G>A
|
NP_001381917.1:p.Arg591Gln
|
|
NM_001394989.1:c.1718G>A
|
NP_001381918.1:p.Arg573Gln
|
|