ENST00000460843.6:c.1972G>T
MANE Select
|
ENSP00000417980.1:p.Glu658Ter
|
|
ENST00000636027.1:c.1858G>T
|
ENSP00000489961.1:p.Glu620Ter
|
|
ENST00000637161.1:c.1879G>T
|
ENSP00000490328.1:p.Glu627Ter
|
|
ENST00000637261.1:c.2012G>T
|
ENSP00000490815.1:n.2012G>T
|
|
ENST00000638071.1:c.1599G>T
|
|
|
ENST00000640639.1:c.1141G>T
|
ENSP00000491823.1:p.Glu381Ter
|
|
ENST00000371394.6:c.*1707G>T
|
ENSP00000485945.1:n.*1707G>T
|
|
ENST00000460843.5:c.1972G>T
|
ENSP00000417980.1:p.Glu658Ter
|
|
ENST00000462484.5:c.1972G>T
|
ENSP00000417328.1:p.Glu658Ter
|
|
ENST00000462942.3:c.829G>T
|
ENSP00000436107.1:p.Glu277Ter
|
|
ENST00000626603.1:n.1651C>A
|
|
|
NM_001145527.1:c.1972G>T
|
NP_001138999.1:p.Glu658Ter
|
|
NM_024757.4:c.1972G>T
|
NP_079033.4:p.Glu658Ter
|
|
XM_005266105.3:c.1963G>T
|
XP_005266162.1:p.Glu655Ter
|
|
XM_005266110.1:c.1879G>T
|
XP_005266167.1:p.Glu627Ter
|
|
XM_006717288.2:c.1954G>T
|
XP_006717351.1:p.Glu652Ter
|
|
XM_011519021.1:c.1981G>T
|
XP_011517323.1:p.Glu661Ter
|
|
XM_011519022.1:c.1978G>T
|
XP_011517324.1:p.Glu660Ter
|
|
XM_011519023.1:c.1960G>T
|
XP_011517325.1:p.Glu654Ter
|
|
XM_011519024.1:c.1903G>T
|
XP_011517326.1:p.Glu635Ter
|
|
XM_011519025.1:c.1879G>T
|
XP_011517327.1:p.Glu627Ter
|
|
XM_011519026.1:c.1837G>T
|
XP_011517328.1:p.Glu613Ter
|
|
XM_011519027.1:c.1981G>T
|
XP_011517329.1:p.Glu661Ter
|
|
XM_011519028.1:c.1981G>T
|
XP_011517330.1:p.Glu661Ter
|
|
XM_011519029.1:c.403G>T
|
XP_011517331.1:p.Glu135Ter
|
|
XM_011519033.1:c.1816G>T
|
XP_011517335.1:p.Glu606Ter
|
|
NM_001354259.1:c.1879G>T
|
NP_001341188.1:p.Glu627Ter
|
|
NM_001354263.1:c.1951G>T
|
NP_001341192.1:p.Glu651Ter
|
|
XM_005266105.5:c.1963G>T
|
XP_005266162.1:p.Glu655Ter
|
|
XM_011519021.3:c.1981G>T
|
XP_011517323.1:p.Glu661Ter
|
|
XM_011519022.3:c.1978G>T
|
XP_011517324.1:p.Glu660Ter
|
|
XM_011519023.3:c.1960G>T
|
XP_011517325.1:p.Glu654Ter
|
|
XM_011519029.3:c.403G>T
|
XP_011517331.1:p.Glu135Ter
|
|
XM_017015134.1:c.1957G>T
|
XP_016870623.1:p.Glu653Ter
|
|
XM_017015136.2:c.1873G>T
|
XP_016870625.1:p.Glu625Ter
|
|
XM_017015137.1:c.1858G>T
|
XP_016870626.1:p.Glu620Ter
|
|
XM_017015138.1:c.1858G>T
|
XP_016870627.1:p.Glu620Ter
|
|
XM_024447674.1:c.1801G>T
|
XP_024303442.1:p.Glu601Ter
|
|
XM_024447675.1:c.1735G>T
|
XP_024303443.1:p.Glu579Ter
|
|
XM_024447676.1:c.1096G>T
|
XP_024303444.1:p.Glu366Ter
|
|
XM_024447677.1:c.1096G>T
|
XP_024303445.1:p.Glu366Ter
|
|
XM_024447678.1:c.1879G>T
|
XP_024303446.1:p.Glu627Ter
|
|
XM_024447679.1:c.1879G>T
|
XP_024303447.1:p.Glu627Ter
|
|
XM_024447680.1:c.1714G>T
|
XP_024303448.1:p.Glu572Ter
|
|
NM_024757.5:c.1972G>T
MANE Select
|
NP_079033.4:p.Glu658Ter
|
|
NM_001145527.2:c.1972G>T
|
NP_001138999.1:p.Glu658Ter
|
|
NM_001354259.2:c.1879G>T
|
NP_001341188.1:p.Glu627Ter
|
|
NM_001354263.2:c.1951G>T
|
NP_001341192.1:p.Glu651Ter
|
|