|
ENST00000314589.11:c.842C>T
|
ENSP00000324443.5:p.Ala281Val
|
|
|
ENST00000687384.1:c.839C>T
|
ENSP00000510225.1:p.Ala280Val
|
|
|
ENST00000689390.1:n.1064C>T
|
|
|
|
ENST00000693031.1:c.815C>T
|
ENSP00000509845.1:p.Ala272Val
|
|
|
ENST00000693549.1:c.842C>T
|
ENSP00000509358.1:p.Ala281Val
|
|
|
ENST00000314589.10:c.842C>T
|
ENSP00000324443.5:p.Ala281Val
|
|
|
ENST00000352241.9:c.908C>T
MANE Select
|
ENSP00000295600.8:p.Ala303Val
|
|
|
ENST00000394351.9:c.587C>T
MANE Plus Clinical
|
ENSP00000377880.3:p.Ala196Val
|
|
|
ENST00000448226.9:c.887C>T
|
ENSP00000391803.3:p.Ala296Val
|
|
|
ENST00000642352.1:c.890C>T
|
ENSP00000494105.1:p.Ala297Val
|
|
|
ENST00000314557.10:c.569C>T
|
ENSP00000324246.6:p.Ala190Val
|
|
|
ENST00000314589.9:c.842C>T
|
ENSP00000324443.5:p.Ala281Val
|
|
|
ENST00000328528.10:c.887C>T
|
ENSP00000327867.6:p.Ala296Val
|
|
|
ENST00000352241.8:c.890C>T
|
ENSP00000295600.7:p.Ala297Val
|
|
|
ENST00000394351.7:c.587C>T
|
ENSP00000377880.3:p.Ala196Val
|
|
|
ENST00000448226.6:c.908C>T
|
ENSP00000391803.2:p.Ala303Val
|
|
|
ENST00000451708.5:c.860C>T
|
ENSP00000398639.1:p.Ala287Val
|
|
|
ENST00000472437.5:c.734C>T
|
ENSP00000418845.1:p.Ala245Val
|
|
|
ENST00000478490.5:c.*234C>T
|
ENSP00000433487.1:n.*234C>T
|
|
|
ENST00000531774.1:c.401C>T
|
ENSP00000435909.1:p.Ala134Val
|
|
|
NM_000248.3:c.587C>T , LRG_776t1:c.587C>T
|
NP_000239.1:p.Ala196Val
|
|
|
NM_001184967.1:c.734C>T
|
NP_001171896.1:p.Ala245Val
|
|
|
NM_006722.2:c.887C>T
|
NP_006713.1:p.Ala296Val
|
|
|
NM_198158.2:c.569C>T
|
NP_937801.1:p.Ala190Val
|
|
|
NM_198159.2:c.890C>T
|
NP_937802.1:p.Ala297Val
|
|
|
NM_198177.2:c.842C>T
|
NP_937820.1:p.Ala281Val
|
|
|
NM_198178.2:c.401C>T
|
NP_937821.2:p.Ala134Val
|
|
|
XM_005264754.1:c.908C>T
|
XP_005264811.1:p.Ala303Val
|
|
|
XM_005264755.2:c.860C>T
|
XP_005264812.1:p.Ala287Val
|
|
|
XM_006713164.2:c.752C>T
|
XP_006713227.1:p.Ala251Val
|
|
|
XM_011533722.1:c.905C>T
|
XP_011532024.1:p.Ala302Val
|
|
|
XM_011533723.1:c.857C>T
|
XP_011532025.1:p.Ala286Val
|
|
|
XM_011533724.1:c.752C>T
|
XP_011532026.1:p.Ala251Val
|
|
|
XM_011533725.1:c.740C>T
|
XP_011532027.1:p.Ala247Val
|
|
|
XM_011533726.1:c.722C>T
|
XP_011532028.1:p.Ala241Val
|
|
|
NM_001354604.1:c.908C>T
|
NP_001341533.1:p.Ala303Val
|
|
|
NM_001354605.1:c.905C>T
|
NP_001341534.1:p.Ala302Val
|
|
|
NM_001354606.1:c.887C>T
|
NP_001341535.1:p.Ala296Val
|
|
|
NM_001354607.1:c.839C>T
|
NP_001341536.1:p.Ala280Val
|
|
|
NM_001354608.1:c.734C>T
|
NP_001341537.1:p.Ala245Val
|
|
|
NM_001184967.2:c.734C>T
|
NP_001171896.1:p.Ala245Val
|
|
|
NM_001354604.2:c.908C>T
MANE Select
|
NP_001341533.1:p.Ala303Val
|
|
|
NM_001354605.2:c.905C>T
|
NP_001341534.1:p.Ala302Val
|
|
|
NM_001354606.2:c.887C>T
|
NP_001341535.1:p.Ala296Val
|
|
|
NM_001354607.2:c.839C>T
|
NP_001341536.1:p.Ala280Val
|
|
|
NM_001354608.2:c.734C>T
|
NP_001341537.1:p.Ala245Val
|
|
|
NM_198158.3:c.569C>T
|
NP_937801.1:p.Ala190Val
|
|
|
NM_198159.3:c.890C>T
|
NP_937802.1:p.Ala297Val
|
|
|
NM_198177.3:c.842C>T
|
NP_937820.1:p.Ala281Val
|
|
|
NM_198178.3:c.401C>T
|
NP_937821.2:p.Ala134Val
|
|
|
NM_000248.4:c.587C>T
MANE Plus Clinical
|
NP_000239.1:p.Ala196Val
|
|
|
NM_006722.3:c.887C>T
|
NP_006713.1:p.Ala296Val
|
|
