|
ENST00000398165.8:c.1358G>C
MANE Select
|
ENSP00000381231.4:p.Gly453Ala
|
|
|
ENST00000352178.9:c.1358G>C
|
ENSP00000344460.5:p.Gly453Ala
|
|
|
ENST00000359624.7:c.1358G>C
|
ENSP00000352643.3:p.Gly453Ala
|
|
|
ENST00000398158.5:c.1358G>C
|
ENSP00000381225.1:p.Gly453Ala
|
|
|
ENST00000398165.7:c.1358G>C
|
ENSP00000381231.3:p.Gly453Ala
|
|
|
ENST00000430013.1:c.319G>C
|
|
|
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ENST00000451248.5:c.108G>C
|
|
|
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ENST00000458223.5:c.121G>C
|
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ENST00000461686.5:n.1669G>C
|
|
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ENST00000462349.5:n.649G>C
|
|
|
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ENST00000491776.1:n.293G>C
|
|
|
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NM_000071.2:c.1358G>C , LRG_777t1:c.1358G>C
|
NP_000062.1:p.Gly453Ala
|
|
|
NM_001178008.1:c.1358G>C
|
NP_001171479.1:p.Gly453Ala
|
|
|
NM_001178009.1:c.1358G>C
|
NP_001171480.1:p.Gly453Ala
|
|
|
XM_011529773.1:c.1409G>C
|
XP_011528075.1:p.Gly470Ala
|
|
|
XM_011529774.1:c.1409G>C
|
XP_011528076.1:p.Gly470Ala
|
|
|
XM_011529775.1:c.1409G>C
|
XP_011528077.1:p.Gly470Ala
|
|
|
XM_011529776.1:c.1409G>C
|
XP_011528078.1:p.Gly470Ala
|
|
|
XM_011529777.1:c.1358G>C
|
XP_011528079.1:p.Gly453Ala
|
|
|
XM_011529778.1:c.1358G>C
|
XP_011528080.1:p.Gly453Ala
|
|
|
XM_011529779.1:c.1358G>C
|
XP_011528081.1:p.Gly453Ala
|
|
|
XM_011529781.1:c.1358G>C
|
XP_011528083.1:p.Gly453Ala
|
|
|
XM_011529782.1:c.1358G>C
|
XP_011528084.1:p.Gly453Ala
|
|
|
XM_011529783.1:c.1043G>C
|
XP_011528085.1:p.Gly348Ala
|
|
|
XM_011529784.1:c.1043G>C
|
XP_011528086.1:p.Gly348Ala
|
|
|
NM_001178008.2:c.1358G>C
|
NP_001171479.1:p.Gly453Ala
|
|
|
NM_001178009.2:c.1358G>C
|
NP_001171480.1:p.Gly453Ala
|
|
|
NM_001320298.1:c.1358G>C
|
NP_001307227.1:p.Gly453Ala
|
|
|
NM_001321072.1:c.1043G>C
|
NP_001308001.1:p.Gly348Ala
|
|
|
XM_011529774.2:c.1409G>C
|
XP_011528076.1:p.Gly470Ala
|
|
|
XM_011529777.2:c.1358G>C
|
XP_011528079.1:p.Gly453Ala
|
|
|
XM_011529783.2:c.1043G>C
|
XP_011528085.1:p.Gly348Ala
|
|
|
XM_017028491.2:c.1358G>C
|
XP_016883980.1:p.Gly453Ala
|
|
|
XM_024452136.1:c.1409G>C
|
XP_024307904.1:p.Gly470Ala
|
|
|
XM_024452137.1:c.1409G>C
|
XP_024307905.1:p.Gly470Ala
|
|
|
XM_024452138.1:c.1043G>C
|
XP_024307906.1:p.Gly348Ala
|
|
|
XM_024452139.1:c.1043G>C
|
XP_024307907.1:p.Gly348Ala
|
|
|
XM_024452140.1:c.1043G>C
|
XP_024307908.1:p.Gly348Ala
|
|
|
XR_001754915.1:n.1729G>C
|
|
|
|
XR_001754916.2:n.1508G>C
|
|
|
|
XR_001754917.2:n.1508G>C
|
|
|
|
XR_002958634.1:n.2329G>C
|
|
|
|
NM_000071.3:c.1358G>C
MANE Select
|
NP_000062.1:p.Gly453Ala
|
|
|
NM_001178009.3:c.1358G>C
|
NP_001171480.1:p.Gly453Ala
|
|
|
NM_001178008.3:c.1358G>C
|
NP_001171479.1:p.Gly453Ala
|
|
|
NM_001320298.2:c.1358G>C
|
NP_001307227.1:p.Gly453Ala
|
|
