ENST00000373327.5:c.1693C>G
MANE Select
|
ENSP00000362424.4:p.Arg565Gly
|
|
ENST00000373327.4:c.1693C>G
|
ENSP00000362424.4:p.Arg565Gly
|
|
ENST00000391993.7:c.1495C>G
|
ENSP00000375851.3:p.Arg499Gly
|
|
ENST00000462122.1:n.704C>G
|
|
|
ENST00000483951.1:n.41C>G
|
|
|
NM_001139490.1:c.1495C>G
|
NP_001132962.1:p.Arg499Gly
|
|
NM_015650.3:c.1693C>G
|
NP_056465.2:p.Arg565Gly
|
|
XM_006712414.1:c.1492C>G
|
XP_006712477.1:p.Arg498Gly
|
|
XM_011510944.1:c.1795C>G
|
XP_011509246.1:p.Arg599Gly
|
|
XM_011510945.1:c.1756C>G
|
XP_011509247.1:p.Arg586Gly
|
|
XM_011510946.1:c.1723C>G
|
XP_011509248.1:p.Arg575Gly
|
|
XM_011510947.1:c.1663C>G
|
XP_011509249.1:p.Arg555Gly
|
|
XM_011510948.1:c.1597C>G
|
XP_011509250.1:p.Arg533Gly
|
|
XM_011510950.1:c.661C>G
|
XP_011509252.1:p.Arg221Gly
|
|
XR_922902.1:n.1992C>G
|
|
|
XM_006712414.2:c.1492C>G
|
XP_006712477.1:p.Arg498Gly
|
|
XM_011510944.2:c.1795C>G
|
XP_011509246.1:p.Arg599Gly
|
|
XM_011510945.2:c.1756C>G
|
XP_011509247.1:p.Arg586Gly
|
|
XM_011510946.2:c.1723C>G
|
XP_011509248.1:p.Arg575Gly
|
|
XM_011510947.2:c.1663C>G
|
XP_011509249.1:p.Arg555Gly
|
|
XM_011510948.2:c.1597C>G
|
XP_011509250.1:p.Arg533Gly
|
|
XM_011510950.2:c.661C>G
|
XP_011509252.1:p.Arg221Gly
|
|
XM_017003789.1:c.1792C>G
|
XP_016859278.1:p.Arg598Gly
|
|
XR_001738696.1:n.1521C>G
|
|
|
XR_001738697.1:n.1518C>G
|
|
|
XR_922902.2:n.2055C>G
|
|
|
NM_015650.4:c.1693C>G
MANE Select
|
NP_056465.2:p.Arg565Gly
|
|