ENST00000373327.5:c.1802G>T
MANE Select
|
ENSP00000362424.4:p.Gly601Val
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ENST00000373327.4:c.1802G>T
|
ENSP00000362424.4:p.Gly601Val
|
|
ENST00000391993.7:c.1604G>T
|
ENSP00000375851.3:p.Gly535Val
|
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ENST00000462122.1:n.813G>T
|
|
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ENST00000483951.1:n.150G>T
|
|
|
NM_001139490.1:c.1604G>T
|
NP_001132962.1:p.Gly535Val
|
|
NM_015650.3:c.1802G>T
|
NP_056465.2:p.Gly601Val
|
|
XM_006712414.1:c.1601G>T
|
XP_006712477.1:p.Gly534Val
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|
XM_011510944.1:c.1904G>T
|
XP_011509246.1:p.Gly635Val
|
|
XM_011510945.1:c.1865G>T
|
XP_011509247.1:p.Gly622Val
|
|
XM_011510946.1:c.1832G>T
|
XP_011509248.1:p.Gly611Val
|
|
XM_011510947.1:c.1772G>T
|
XP_011509249.1:p.Gly591Val
|
|
XM_011510948.1:c.1706G>T
|
XP_011509250.1:p.Gly569Val
|
|
XM_011510950.1:c.770G>T
|
XP_011509252.1:p.Gly257Val
|
|
XM_006712414.2:c.1601G>T
|
XP_006712477.1:p.Gly534Val
|
|
XM_011510944.2:c.1904G>T
|
XP_011509246.1:p.Gly635Val
|
|
XM_011510945.2:c.1865G>T
|
XP_011509247.1:p.Gly622Val
|
|
XM_011510946.2:c.1832G>T
|
XP_011509248.1:p.Gly611Val
|
|
XM_011510947.2:c.1772G>T
|
XP_011509249.1:p.Gly591Val
|
|
XM_011510948.2:c.1706G>T
|
XP_011509250.1:p.Gly569Val
|
|
XM_011510950.2:c.770G>T
|
XP_011509252.1:p.Gly257Val
|
|
XM_017003789.1:c.1901G>T
|
XP_016859278.1:p.Gly634Val
|
|
XR_001738696.1:n.1630G>T
|
|
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XR_001738697.1:n.1627G>T
|
|
|
NM_015650.4:c.1802G>T
MANE Select
|
NP_056465.2:p.Gly601Val
|
|