ENST00000356141.9:c.1807A>G
MANE Select
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ENSP00000348460.4:p.Arg603Gly
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ENST00000551634.6:c.1816A>G
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ENSP00000448373.2:p.Arg606Gly
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ENST00000680362.1:c.1707A>G
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ENST00000681323.1:c.793+2533A>G
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ENST00000346562.6:c.1711A>G
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ENSP00000319610.5:p.Arg571Gly
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ENST00000356141.8:c.1807A>G
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ENSP00000348460.4:p.Arg603Gly
|
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ENST00000357798.9:c.1768A>G
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ENSP00000350446.5:p.Arg590Gly
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ENST00000548645.5:c.1717A>G
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ENSP00000448916.1:p.Arg573Gly
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ENST00000551492.5:c.1822A>G
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ENSP00000450392.1:p.Arg608Gly
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ENST00000551634.5:c.1729A>G
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ENSP00000448373.1:p.Arg577Gly
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NM_001164749.1:c.1807A>G
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NP_001158221.1:p.Arg603Gly
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NM_001165893.1:c.1717A>G
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NP_001159365.1:p.Arg573Gly
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NM_022123.2:c.1711A>G
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NP_071406.1:p.Arg571Gly
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NM_173159.2:c.1768A>G
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NP_775182.1:p.Arg590Gly
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XM_005267991.2:c.1828A>G
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XP_005268048.1:p.Arg610Gly
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XM_005267992.2:c.1822A>G
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XP_005268049.1:p.Arg608Gly
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XM_005267993.2:c.1768A>G
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XP_005268050.1:p.Arg590Gly
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XM_011537067.1:c.1858A>G
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XP_011535369.1:p.Arg620Gly
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XM_011537068.1:c.1849A>G
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XP_011535370.1:p.Arg617Gly
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XM_011537069.1:c.1819A>G
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XP_011535371.1:p.Arg607Gly
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XM_011537070.1:c.1762A>G
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XP_011535372.1:p.Arg588Gly
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XM_011537071.1:c.1729A>G
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XP_011535373.1:p.Arg577Gly
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XM_011537072.1:c.1708A>G
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XP_011535374.1:p.Arg570Gly
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XM_011537073.1:c.1501A>G
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XP_011535375.1:p.Arg501Gly
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XM_011537074.1:c.1501A>G
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XP_011535376.1:p.Arg501Gly
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XM_005267991.3:c.1915A>G
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XP_005268048.2:p.Arg639Gly
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XM_005267992.3:c.1909A>G
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XP_005268049.2:p.Arg637Gly
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XM_011537067.2:c.1858A>G
|
XP_011535369.1:p.Arg620Gly
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XM_011537069.2:c.1906A>G
|
XP_011535371.2:p.Arg636Gly
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XM_011537070.2:c.1762A>G
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XP_011535372.1:p.Arg588Gly
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XM_011537071.2:c.1816A>G
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XP_011535373.2:p.Arg606Gly
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XM_011537072.2:c.1708A>G
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XP_011535374.1:p.Arg570Gly
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XM_017021582.1:c.1966A>G
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XP_016877071.1:p.Arg656Gly
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XM_017021583.1:c.1957A>G
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XP_016877072.1:p.Arg653Gly
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XM_017021584.1:c.1876A>G
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XP_016877073.1:p.Arg626Gly
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XM_017021585.1:c.1825A>G
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XP_016877074.1:p.Arg609Gly
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XM_017021586.1:c.1501A>G
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XP_016877075.1:p.Arg501Gly
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XM_017021587.1:c.1501A>G
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XP_016877076.1:p.Arg501Gly
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XM_017021588.1:c.1501A>G
|
XP_016877077.1:p.Arg501Gly
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NM_001164749.2:c.1807A>G
MANE Select
|
NP_001158221.1:p.Arg603Gly
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NM_001165893.2:c.1717A>G
|
NP_001159365.1:p.Arg573Gly
|
|
NM_022123.3:c.1711A>G
|
NP_071406.1:p.Arg571Gly
|
|
NM_173159.3:c.1768A>G
|
NP_775182.1:p.Arg590Gly
|
|
NM_001394988.1:c.1762A>G
|
NP_001381917.1:p.Arg588Gly
|
|
NM_001394989.1:c.1708A>G
|
NP_001381918.1:p.Arg570Gly
|
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