ENST00000405460.9:c.10789G=
MANE Select
|
ENSP00000384582.2:p.Glu3597=
|
|
ENST00000639431.1:c.265+69401G=
|
ENSP00000491057.1:n.265+69401G=
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ENST00000640374.1:n.3933G=
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|
|
ENST00000640464.1:n.1208G=
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|
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ENST00000405460.6:c.10789G=
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ENSP00000384582.2:p.Glu3597=
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|
ENST00000509621.1:c.3486G=
|
|
|
NM_032119.3:c.10789G=
|
NP_115495.3:p.Glu3597=
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|
NR_003149.1:n.10802G=
|
|
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XM_011543675.1:c.10786G=
|
XP_011541977.1:p.Glu3596=
|
|
XM_011543676.1:c.10708G=
|
XP_011541978.1:p.Glu3570=
|
|
XM_011543677.1:c.8092G=
|
XP_011541979.1:p.Glu2698=
|
|
XM_011543678.1:c.10789G=
|
XP_011541980.1:p.Glu3597=
|
|
XM_011543679.1:c.*11G=
|
XP_011541981.1:n.*11G=
|
|
NM_032119.4:c.10789G=
MANE Select
|
NP_115495.3:p.Glu3597=
|
|
XM_017009963.2:c.10810G=
|
XP_016865452.1:p.Glu3604=
|
|
XM_017009964.2:c.10807G=
|
XP_016865453.1:p.Glu3603=
|
|
XM_017009965.1:c.10807G=
|
XP_016865454.1:p.Glu3603=
|
|
XM_017009966.2:c.10729G=
|
XP_016865455.1:p.Glu3577=
|
|
XM_017009967.1:c.10714G=
|
XP_016865456.1:p.Glu3572=
|
|
XM_017009968.2:c.10810G=
|
XP_016865457.1:p.Glu3604=
|
|
XM_017009969.2:c.10810G=
|
XP_016865458.1:p.Glu3604=
|
|
XM_017009970.2:c.10810G=
|
XP_016865459.1:p.Glu3604=
|
|
XM_017009971.2:c.10810G=
|
XP_016865460.1:p.Glu3604=
|
|
XM_017009972.1:c.3928G=
|
XP_016865461.1:p.Glu1310=
|
|
XM_017009973.1:c.3907G=
|
XP_016865462.1:p.Glu1303=
|
|
XM_017009974.2:c.*11G=
|
XP_016865463.1:n.*11G=
|
|
NR_003149.2:n.10805G=
|
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