ENST00000682266.1:c.1468A>G
|
ENSP00000507766.1:p.Arg490Gly
|
|
ENST00000682341.1:c.1876A>G
|
ENSP00000508251.1:p.Arg626Gly
|
|
ENST00000683197.1:c.1876A>G
|
ENSP00000507641.1:p.Arg626Gly
|
|
ENST00000683411.1:c.1468A>G
|
ENSP00000508397.1:p.Arg490Gly
|
|
ENST00000683437.1:c.1468A>G
|
ENSP00000508408.1:p.Arg490Gly
|
|
ENST00000683613.1:n.2912A>G
|
|
|
ENST00000684663.1:c.1873A>G
|
ENSP00000508009.1:p.Arg625Gly
|
|
ENST00000324559.9:c.1918A>G
MANE Select
|
ENSP00000315371.9:p.Arg640Gly
|
|
ENST00000648804.1:n.2253A>G
|
|
|
ENST00000324559.8:c.1918A>G
|
ENSP00000315371.8:p.Arg640Gly
|
|
NM_001142649.1:c.1915A>G
|
NP_001136121.1:p.Arg639Gly
|
|
NM_213599.2:c.1918A>G , LRG_868t1:c.1918A>G
|
NP_998764.1:p.Arg640Gly
|
|
XM_005252820.2:c.1876A>G
|
XP_005252877.2:p.Arg626Gly
|
|
XM_005252821.2:c.1873A>G
|
XP_005252878.2:p.Arg625Gly
|
|
XM_005252822.3:c.1840A>G
|
XP_005252879.1:p.Arg614Gly
|
|
XM_005252823.3:c.1837A>G
|
XP_005252880.1:p.Arg613Gly
|
|
XM_011519949.1:c.1825A>G
|
XP_011518251.1:p.Arg609Gly
|
|
XM_005252820.3:c.1876A>G
|
XP_005252877.2:p.Arg626Gly
|
|
XM_005252821.3:c.1873A>G
|
XP_005252878.2:p.Arg625Gly
|
|
XM_005252822.4:c.1840A>G
|
XP_005252879.1:p.Arg614Gly
|
|
XM_011519949.2:c.1825A>G
|
XP_011518251.1:p.Arg609Gly
|
|
NM_001142649.2:c.1915A>G
|
NP_001136121.1:p.Arg639Gly
|
|
NM_213599.3:c.1918A>G
MANE Select
|
NP_998764.1:p.Arg640Gly
|
|