|
ENST00000540033.3:c.1933C>G
|
ENSP00000440826.2:p.Arg645Gly
|
|
|
ENST00000706843.1:c.1924C>G
|
ENSP00000516584.1:p.Arg642Gly
|
|
|
ENST00000706845.1:c.*1781C>G
|
ENSP00000516587.1:n.*1781C>G
|
|
|
ENST00000706846.1:c.1948C>G
|
ENSP00000516588.1:p.Arg650Gly
|
|
|
ENST00000706867.1:c.2029C>G
|
ENSP00000516594.1:p.Arg677Gly
|
|
|
ENST00000706868.1:c.1948C>G
|
ENSP00000516595.1:p.Arg650Gly
|
|
|
ENST00000706869.1:n.310-3808C>G
|
|
|
|
ENST00000706883.1:c.736C>G
|
ENSP00000516600.1:p.Arg246Gly
|
|
|
ENST00000706885.1:c.1813C>G
|
ENSP00000516601.1:p.Arg605Gly
|
|
|
ENST00000684568.2:c.1948C>G
MANE Select
|
ENSP00000506999.1:p.Arg650Gly
|
|
|
ENST00000370331.5:c.1900C>G
|
ENSP00000359356.1:p.Arg634Gly
|
|
|
ENST00000491940.5:n.753C>G
|
|
|
|
ENST00000492513.5:n.421C>G
|
|
|
|
ENST00000540033.2:c.1933C>G
|
ENSP00000440826.2:p.Arg645Gly
|
|
|
NM_001308248.1:c.1933C>G
|
NP_001295177.1:p.Arg645Gly
|
|
|
NM_005665.4:c.1900C>G
|
NP_005656.4:p.Arg634Gly
|
|
|
NM_005665.5:c.1900C>G
|
NP_005656.4:p.Arg634Gly
|
|
|
XM_011542099.1:c.2152C>G
|
XP_011540401.1:p.Arg718Gly
|
|
|
XM_011542100.1:c.2152C>G
|
XP_011540402.1:p.Arg718Gly
|
|
|
XM_011542101.1:c.2029C>G
|
XP_011540403.1:p.Arg677Gly
|
|
|
XM_011542102.1:c.2005C>G
|
XP_011540404.1:p.Arg669Gly
|
|
|
XM_011542103.1:c.2032-2205C>G
|
XP_011540405.1:n.2032-2205C>G
|
|
|
XM_011542104.1:c.1993C>G
|
XP_011540406.1:p.Arg665Gly
|
|
|
XM_011542105.1:c.1972C>G
|
XP_011540407.1:p.Arg658Gly
|
|
|
XM_011542107.1:c.1900C>G
|
XP_011540409.1:p.Arg634Gly
|
|
|
XM_011542108.1:c.2152C>G
|
XP_011540410.1:p.Arg718Gly
|
|
|
XM_011542109.1:c.2152C>G
|
XP_011540411.1:p.Arg718Gly
|
|
|
NM_001350197.1:c.1948C>G
|
NP_001337126.1:p.Arg650Gly
|
|
|
NM_001350198.1:c.1948C>G
|
NP_001337127.1:p.Arg650Gly
|
|
|
XM_017002269.1:c.2161C>G
|
XP_016857758.1:p.Arg721Gly
|
|
|
XM_017002270.2:c.2152C>G
|
XP_016857759.1:p.Arg718Gly
|
|
|
XM_017002271.2:c.2080C>G
|
XP_016857760.1:p.Arg694Gly
|
|
|
XM_017002272.1:c.2161C>G
|
XP_016857761.1:p.Arg721Gly
|
|
|
XM_017002273.2:c.2029C>G
|
XP_016857762.1:p.Arg677Gly
|
|
|
XM_017002274.1:c.2029C>G
|
XP_016857763.1:p.Arg677Gly
|
|
|
XM_017002275.1:c.2029C>G
|
XP_016857764.1:p.Arg677Gly
|
|
|
XM_017002276.2:c.1948C>G
|
XP_016857765.1:p.Arg650Gly
|
|
|
XM_017002277.1:c.1933C>G
|
XP_016857766.1:p.Arg645Gly
|
|
|
XM_017002278.1:c.2014C>G
|
XP_016857767.1:p.Arg672Gly
|
|
|
XM_017002279.1:c.1894C>G
|
XP_016857768.1:p.Arg632Gly
|
|
|
XM_017002281.2:c.1924C>G
|
XP_016857770.1:p.Arg642Gly
|
|
|
XM_017002282.1:c.2161C>G
|
XP_016857771.1:p.Arg721Gly
|
|
|
XM_017002283.1:c.2080C>G
|
XP_016857772.1:p.Arg694Gly
|
|
|
XM_017002284.2:c.1801C>G
|
XP_016857773.1:p.Arg601Gly
|
|
|
XM_017002286.2:c.1537C>G
|
XP_016857775.1:p.Arg513Gly
|
|
|
XM_017002287.2:c.1537C>G
|
XP_016857776.1:p.Arg513Gly
|
|
|
XM_017002288.1:c.1537C>G
|
XP_016857777.1:p.Arg513Gly
|
|
|
XM_024449686.1:c.2080C>G
|
XP_024305454.1:p.Arg694Gly
|
|
|
XM_024449689.1:c.1981C>G
|
XP_024305457.1:p.Arg661Gly
|
|
|
XM_024449690.1:c.1813C>G
|
XP_024305458.1:p.Arg605Gly
|
|
|
NM_001308248.2:c.1933C>G
|
NP_001295177.1:p.Arg645Gly
|
|
|
NM_001350197.2:c.1948C>G
MANE Select
|
NP_001337126.1:p.Arg650Gly
|
|
|
NM_001350198.2:c.1948C>G
|
NP_001337127.1:p.Arg650Gly
|
|
|
NM_001377210.1:c.1924C>G
|
NP_001364139.1:p.Arg642Gly
|
|
|
NM_001377211.1:c.1906C>G
|
NP_001364140.1:p.Arg636Gly
|
|
|
NM_001377212.1:c.1801C>G
|
NP_001364141.1:p.Arg601Gly
|
|
|
NM_001377213.1:c.2029C>G
|
NP_001364142.1:p.Arg677Gly
|
|
|
NM_005665.6:c.1900C>G
|
NP_005656.4:p.Arg634Gly
|
|
