|
ENST00000314589.11:c.1396G>T
|
ENSP00000324443.5:p.Asp466Tyr
|
|
|
ENST00000687384.1:c.1393G>T
|
ENSP00000510225.1:p.Asp465Tyr
|
|
|
ENST00000689390.1:n.1618G>T
|
|
|
|
ENST00000693031.1:c.1369G>T
|
ENSP00000509845.1:p.Asp457Tyr
|
|
|
ENST00000693549.1:c.*207G>T
|
ENSP00000509358.1:n.*207G>T
|
|
|
ENST00000314589.10:c.1396G>T
|
ENSP00000324443.5:p.Asp466Tyr
|
|
|
ENST00000352241.9:c.1462G>T
MANE Select
|
ENSP00000295600.8:p.Asp488Tyr
|
|
|
ENST00000394351.9:c.1141G>T
MANE Plus Clinical
|
ENSP00000377880.3:p.Asp381Tyr
|
|
|
ENST00000448226.9:c.1441G>T
|
ENSP00000391803.3:p.Asp481Tyr
|
|
|
ENST00000642352.1:c.1444G>T
|
ENSP00000494105.1:p.Asp482Tyr
|
|
|
ENST00000314557.10:c.1123G>T
|
ENSP00000324246.6:p.Asp375Tyr
|
|
|
ENST00000314589.9:c.1396G>T
|
ENSP00000324443.5:p.Asp466Tyr
|
|
|
ENST00000328528.10:c.1441G>T
|
ENSP00000327867.6:p.Asp481Tyr
|
|
|
ENST00000352241.8:c.1444G>T
|
ENSP00000295600.7:p.Asp482Tyr
|
|
|
ENST00000394351.7:c.1141G>T
|
ENSP00000377880.3:p.Asp381Tyr
|
|
|
ENST00000448226.6:c.1462G>T
|
ENSP00000391803.2:p.Asp488Tyr
|
|
|
ENST00000472437.5:c.1288G>T
|
ENSP00000418845.1:p.Asp430Tyr
|
|
|
ENST00000478490.5:c.*788G>T
|
ENSP00000433487.1:n.*788G>T
|
|
|
ENST00000531774.1:c.955G>T
|
ENSP00000435909.1:p.Asp319Tyr
|
|
|
NM_000248.3:c.1141G>T , LRG_776t1:c.1141G>T
|
NP_000239.1:p.Asp381Tyr
|
|
|
NM_001184967.1:c.1288G>T
|
NP_001171896.1:p.Asp430Tyr
|
|
|
NM_006722.2:c.1441G>T
|
NP_006713.1:p.Asp481Tyr
|
|
|
NM_198158.2:c.1123G>T
|
NP_937801.1:p.Asp375Tyr
|
|
|
NM_198159.2:c.1444G>T
|
NP_937802.1:p.Asp482Tyr
|
|
|
NM_198177.2:c.1396G>T
|
NP_937820.1:p.Asp466Tyr
|
|
|
NM_198178.2:c.955G>T
|
NP_937821.2:p.Asp319Tyr
|
|
|
XM_005264754.1:c.1462G>T
|
XP_005264811.1:p.Asp488Tyr
|
|
|
XM_005264755.2:c.1414G>T
|
XP_005264812.1:p.Asp472Tyr
|
|
|
XM_006713164.2:c.1306G>T
|
XP_006713227.1:p.Asp436Tyr
|
|
|
XM_011533722.1:c.1459G>T
|
XP_011532024.1:p.Asp487Tyr
|
|
|
XM_011533723.1:c.1411G>T
|
XP_011532025.1:p.Asp471Tyr
|
|
|
XM_011533724.1:c.1306G>T
|
XP_011532026.1:p.Asp436Tyr
|
|
|
XM_011533725.1:c.1294G>T
|
XP_011532027.1:p.Asp432Tyr
|
|
|
XM_011533726.1:c.1276G>T
|
XP_011532028.1:p.Asp426Tyr
|
|
|
NM_001354604.1:c.1462G>T
|
NP_001341533.1:p.Asp488Tyr
|
|
|
NM_001354605.1:c.1459G>T
|
NP_001341534.1:p.Asp487Tyr
|
|
|
NM_001354606.1:c.1441G>T
|
NP_001341535.1:p.Asp481Tyr
|
|
|
NM_001354607.1:c.1393G>T
|
NP_001341536.1:p.Asp465Tyr
|
|
|
NM_001354608.1:c.1288G>T
|
NP_001341537.1:p.Asp430Tyr
|
|
|
NM_001184967.2:c.1288G>T
|
NP_001171896.1:p.Asp430Tyr
|
|
|
NM_001354604.2:c.1462G>T
MANE Select
|
NP_001341533.1:p.Asp488Tyr
|
|
|
NM_001354605.2:c.1459G>T
|
NP_001341534.1:p.Asp487Tyr
|
|
|
NM_001354606.2:c.1441G>T
|
NP_001341535.1:p.Asp481Tyr
|
|
|
NM_001354607.2:c.1393G>T
|
NP_001341536.1:p.Asp465Tyr
|
|
|
NM_001354608.2:c.1288G>T
|
NP_001341537.1:p.Asp430Tyr
|
|
|
NM_198158.3:c.1123G>T
|
NP_937801.1:p.Asp375Tyr
|
|
|
NM_198159.3:c.1444G>T
|
NP_937802.1:p.Asp482Tyr
|
|
|
NM_198177.3:c.1396G>T
|
NP_937820.1:p.Asp466Tyr
|
|
|
NM_198178.3:c.955G>T
|
NP_937821.2:p.Asp319Tyr
|
|
|
NM_000248.4:c.1141G>T
MANE Plus Clinical
|
NP_000239.1:p.Asp381Tyr
|
|
|
NM_006722.3:c.1441G>T
|
NP_006713.1:p.Asp481Tyr
|
|
