ENST00000461526.2:c.755T>G
|
ENSP00000513165.1:p.Val252Gly
|
|
ENST00000697178.1:c.*1504T>G
|
ENSP00000513163.1:n.*1504T>G
|
|
ENST00000697180.1:c.585T>G
|
|
|
ENST00000697241.1:c.512T>G
|
ENSP00000513206.1:p.Val171Gly
|
|
ENST00000389793.7:c.6080T>G
MANE Select
|
ENSP00000374443.2:p.Val2027Gly
|
|
ENST00000389793.6:c.6080T>G
|
ENSP00000374443.2:p.Val2027Gly
|
|
ENST00000389794.7:c.*1504T>G
|
ENSP00000374444.4:n.*1504T>G
|
|
ENST00000489585.5:n.6512+119T>G
|
|
|
NM_000081.3:c.6080T>G , LRG_143t1:c.6080T>G
|
NP_000072.2:p.Val2027Gly
|
|
NM_001301365.1:c.6080T>G , LRG_143t2:c.6080T>G
|
NP_001288294.1:p.Val2027Gly
|
|
XM_011544031.1:c.6080T>G
|
XP_011542333.1:p.Val2027Gly
|
|
XM_011544032.1:c.6080T>G
|
XP_011542334.1:p.Val2027Gly
|
|
XM_011544033.1:c.6080T>G
|
XP_011542335.1:p.Val2027Gly
|
|
XM_011544034.1:c.5942T>G
|
XP_011542336.1:p.Val1981Gly
|
|
XM_011544035.1:c.6080T>G
|
XP_011542337.1:p.Val2027Gly
|
|
XM_011544036.1:c.3743T>G
|
XP_011542338.1:p.Val1248Gly
|
|
XM_011544037.1:c.6080T>G
|
XP_011542339.1:p.Val2027Gly
|
|
XM_011544038.1:c.6080T>G
|
XP_011542340.1:p.Val2027Gly
|
|
XM_011544039.1:c.6080T>G
|
XP_011542341.1:p.Val2027Gly
|
|
XM_011544040.1:c.5989T>G
|
XP_011542342.1:p.Phe1997Val
|
|
XM_011544033.2:c.6080T>G
|
XP_011542335.1:p.Val2027Gly
|
|
XM_011544035.2:c.6080T>G
|
XP_011542337.1:p.Val2027Gly
|
|
XM_011544036.2:c.3743T>G
|
XP_011542338.1:p.Val1248Gly
|
|
XM_011544037.2:c.6080T>G
|
XP_011542339.1:p.Val2027Gly
|
|
XM_011544039.2:c.6080T>G
|
XP_011542341.1:p.Val2027Gly
|
|
XM_017000150.1:c.6080T>G
|
XP_016855639.1:p.Val2027Gly
|
|
XM_017000151.1:c.5851T>G
|
XP_016855640.1:p.Phe1951Val
|
|
XR_001736946.2:n.6262T>G
|
|
|
XR_001736947.1:n.6262T>G
|
|
|
XR_001736948.1:n.6262T>G
|
|
|
XR_002959252.1:n.6171T>G
|
|
|
NM_000081.4:c.6080T>G
MANE Select
|
NP_000072.2:p.Val2027Gly
|
|