|
ENST00000314589.11:c.1359A>T
|
ENSP00000324443.5:p.Thr453=
|
|
|
ENST00000687384.1:c.1356A>T
|
ENSP00000510225.1:p.Thr452=
|
|
|
ENST00000689390.1:n.1581A>T
|
|
|
|
ENST00000693031.1:c.1332A>T
|
ENSP00000509845.1:p.Thr444=
|
|
|
ENST00000693549.1:c.*170A>T
|
ENSP00000509358.1:n.*170A>T
|
|
|
ENST00000314589.10:c.1359A>T
|
ENSP00000324443.5:p.Thr453=
|
|
|
ENST00000352241.9:c.1425A>T
MANE Select
|
ENSP00000295600.8:p.Thr475=
|
|
|
ENST00000394351.9:c.1104A>T
MANE Plus Clinical
|
ENSP00000377880.3:p.Thr368=
|
|
|
ENST00000448226.9:c.1404A>T
|
ENSP00000391803.3:p.Thr468=
|
|
|
ENST00000642352.1:c.1407A>T
|
ENSP00000494105.1:p.Thr469=
|
|
|
ENST00000314557.10:c.1086A>T
|
ENSP00000324246.6:p.Thr362=
|
|
|
ENST00000314589.9:c.1359A>T
|
ENSP00000324443.5:p.Thr453=
|
|
|
ENST00000328528.10:c.1404A>T
|
ENSP00000327867.6:p.Thr468=
|
|
|
ENST00000352241.8:c.1407A>T
|
ENSP00000295600.7:p.Thr469=
|
|
|
ENST00000394351.7:c.1104A>T
|
ENSP00000377880.3:p.Thr368=
|
|
|
ENST00000448226.6:c.1425A>T
|
ENSP00000391803.2:p.Thr475=
|
|
|
ENST00000472437.5:c.1251A>T
|
ENSP00000418845.1:p.Thr417=
|
|
|
ENST00000478490.5:c.*751A>T
|
ENSP00000433487.1:n.*751A>T
|
|
|
ENST00000531774.1:c.918A>T
|
ENSP00000435909.1:p.Thr306=
|
|
|
NM_000248.3:c.1104A>T , LRG_776t1:c.1104A>T
|
NP_000239.1:p.Thr368=
|
|
|
NM_001184967.1:c.1251A>T
|
NP_001171896.1:p.Thr417=
|
|
|
NM_006722.2:c.1404A>T
|
NP_006713.1:p.Thr468=
|
|
|
NM_198158.2:c.1086A>T
|
NP_937801.1:p.Thr362=
|
|
|
NM_198159.2:c.1407A>T
|
NP_937802.1:p.Thr469=
|
|
|
NM_198177.2:c.1359A>T
|
NP_937820.1:p.Thr453=
|
|
|
NM_198178.2:c.918A>T
|
NP_937821.2:p.Thr306=
|
|
|
XM_005264754.1:c.1425A>T
|
XP_005264811.1:p.Thr475=
|
|
|
XM_005264755.2:c.1377A>T
|
XP_005264812.1:p.Thr459=
|
|
|
XM_006713164.2:c.1269A>T
|
XP_006713227.1:p.Thr423=
|
|
|
XM_011533722.1:c.1422A>T
|
XP_011532024.1:p.Thr474=
|
|
|
XM_011533723.1:c.1374A>T
|
XP_011532025.1:p.Thr458=
|
|
|
XM_011533724.1:c.1269A>T
|
XP_011532026.1:p.Thr423=
|
|
|
XM_011533725.1:c.1257A>T
|
XP_011532027.1:p.Thr419=
|
|
|
XM_011533726.1:c.1239A>T
|
XP_011532028.1:p.Thr413=
|
|
|
NM_001354604.1:c.1425A>T
|
NP_001341533.1:p.Thr475=
|
|
|
NM_001354605.1:c.1422A>T
|
NP_001341534.1:p.Thr474=
|
|
|
NM_001354606.1:c.1404A>T
|
NP_001341535.1:p.Thr468=
|
|
|
NM_001354607.1:c.1356A>T
|
NP_001341536.1:p.Thr452=
|
|
|
NM_001354608.1:c.1251A>T
|
NP_001341537.1:p.Thr417=
|
|
|
NM_001184967.2:c.1251A>T
|
NP_001171896.1:p.Thr417=
|
|
|
NM_001354604.2:c.1425A>T
MANE Select
|
NP_001341533.1:p.Thr475=
|
|
|
NM_001354605.2:c.1422A>T
|
NP_001341534.1:p.Thr474=
|
|
|
NM_001354606.2:c.1404A>T
|
NP_001341535.1:p.Thr468=
|
|
|
NM_001354607.2:c.1356A>T
|
NP_001341536.1:p.Thr452=
|
|
|
NM_001354608.2:c.1251A>T
|
NP_001341537.1:p.Thr417=
|
|
|
NM_198158.3:c.1086A>T
|
NP_937801.1:p.Thr362=
|
|
|
NM_198159.3:c.1407A>T
|
NP_937802.1:p.Thr469=
|
|
|
NM_198177.3:c.1359A>T
|
NP_937820.1:p.Thr453=
|
|
|
NM_198178.3:c.918A>T
|
NP_937821.2:p.Thr306=
|
|
|
NM_000248.4:c.1104A>T
MANE Plus Clinical
|
NP_000239.1:p.Thr368=
|
|
|
NM_006722.3:c.1404A>T
|
NP_006713.1:p.Thr468=
|
|
