|
ENST00000314589.11:c.1128G>T
|
ENSP00000324443.5:p.Gln376His
|
|
|
ENST00000687384.1:c.1125G>T
|
ENSP00000510225.1:p.Gln375His
|
|
|
ENST00000689390.1:n.1350G>T
|
|
|
|
ENST00000693031.1:c.1101G>T
|
ENSP00000509845.1:p.Gln367His
|
|
|
ENST00000693549.1:c.1114-53G>T
|
ENSP00000509358.1:n.1114-53G>T
|
|
|
ENST00000314589.10:c.1128G>T
|
ENSP00000324443.5:p.Gln376His
|
|
|
ENST00000352241.9:c.1194G>T
MANE Select
|
ENSP00000295600.8:p.Gln398His
|
|
|
ENST00000394351.9:c.873G>T
MANE Plus Clinical
|
ENSP00000377880.3:p.Gln291His
|
|
|
ENST00000448226.9:c.1173G>T
|
ENSP00000391803.3:p.Gln391His
|
|
|
ENST00000642352.1:c.1176G>T
|
ENSP00000494105.1:p.Gln392His
|
|
|
ENST00000314557.10:c.855G>T
|
ENSP00000324246.6:p.Gln285His
|
|
|
ENST00000314589.9:c.1128G>T
|
ENSP00000324443.5:p.Gln376His
|
|
|
ENST00000328528.10:c.1173G>T
|
ENSP00000327867.6:p.Gln391His
|
|
|
ENST00000352241.8:c.1176G>T
|
ENSP00000295600.7:p.Gln392His
|
|
|
ENST00000394351.7:c.873G>T
|
ENSP00000377880.3:p.Gln291His
|
|
|
ENST00000448226.6:c.1194G>T
|
ENSP00000391803.2:p.Gln398His
|
|
|
ENST00000472437.5:c.1020G>T
|
ENSP00000418845.1:p.Gln340His
|
|
|
ENST00000478490.5:c.*520G>T
|
ENSP00000433487.1:n.*520G>T
|
|
|
ENST00000531774.1:c.687G>T
|
ENSP00000435909.1:p.Gln229His
|
|
|
NM_000248.3:c.873G>T , LRG_776t1:c.873G>T
|
NP_000239.1:p.Gln291His
|
|
|
NM_001184967.1:c.1020G>T
|
NP_001171896.1:p.Gln340His
|
|
|
NM_006722.2:c.1173G>T
|
NP_006713.1:p.Gln391His
|
|
|
NM_198158.2:c.855G>T
|
NP_937801.1:p.Gln285His
|
|
|
NM_198159.2:c.1176G>T
|
NP_937802.1:p.Gln392His
|
|
|
NM_198177.2:c.1128G>T
|
NP_937820.1:p.Gln376His
|
|
|
NM_198178.2:c.687G>T
|
NP_937821.2:p.Gln229His
|
|
|
XM_005264754.1:c.1194G>T
|
XP_005264811.1:p.Gln398His
|
|
|
XM_005264755.2:c.1146G>T
|
XP_005264812.1:p.Gln382His
|
|
|
XM_006713164.2:c.1038G>T
|
XP_006713227.1:p.Gln346His
|
|
|
XM_011533722.1:c.1191G>T
|
XP_011532024.1:p.Gln397His
|
|
|
XM_011533723.1:c.1143G>T
|
XP_011532025.1:p.Gln381His
|
|
|
XM_011533724.1:c.1038G>T
|
XP_011532026.1:p.Gln346His
|
|
|
XM_011533725.1:c.1026G>T
|
XP_011532027.1:p.Gln342His
|
|
|
XM_011533726.1:c.1008G>T
|
XP_011532028.1:p.Gln336His
|
|
|
NM_001354604.1:c.1194G>T
|
NP_001341533.1:p.Gln398His
|
|
|
NM_001354605.1:c.1191G>T
|
NP_001341534.1:p.Gln397His
|
|
|
NM_001354606.1:c.1173G>T
|
NP_001341535.1:p.Gln391His
|
|
|
NM_001354607.1:c.1125G>T
|
NP_001341536.1:p.Gln375His
|
|
|
NM_001354608.1:c.1020G>T
|
NP_001341537.1:p.Gln340His
|
|
|
NM_001184967.2:c.1020G>T
|
NP_001171896.1:p.Gln340His
|
|
|
NM_001354604.2:c.1194G>T
MANE Select
|
NP_001341533.1:p.Gln398His
|
|
|
NM_001354605.2:c.1191G>T
|
NP_001341534.1:p.Gln397His
|
|
|
NM_001354606.2:c.1173G>T
|
NP_001341535.1:p.Gln391His
|
|
|
NM_001354607.2:c.1125G>T
|
NP_001341536.1:p.Gln375His
|
|
|
NM_001354608.2:c.1020G>T
|
NP_001341537.1:p.Gln340His
|
|
|
NM_198158.3:c.855G>T
|
NP_937801.1:p.Gln285His
|
|
|
NM_198159.3:c.1176G>T
|
NP_937802.1:p.Gln392His
|
|
|
NM_198177.3:c.1128G>T
|
NP_937820.1:p.Gln376His
|
|
|
NM_198178.3:c.687G>T
|
NP_937821.2:p.Gln229His
|
|
|
NM_000248.4:c.873G>T
MANE Plus Clinical
|
NP_000239.1:p.Gln291His
|
|
|
NM_006722.3:c.1173G>T
|
NP_006713.1:p.Gln391His
|
|
