ENST00000405460.9:c.11505T>A
MANE Select
|
ENSP00000384582.2:p.Asp3835Glu
|
|
ENST00000425867.3:c.636T>A
|
ENSP00000392618.3:p.Asp212Glu
|
|
ENST00000639431.1:c.265+78901T>A
|
ENSP00000491057.1:n.265+78901T>A
|
|
ENST00000640374.1:n.4649T>A
|
|
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ENST00000640464.1:n.1924T>A
|
|
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ENST00000405460.6:c.11505T>A
|
ENSP00000384582.2:p.Asp3835Glu
|
|
ENST00000509621.1:c.4202T>A
|
|
|
NM_032119.3:c.11505T>A
|
NP_115495.3:p.Asp3835Glu
|
|
NR_003149.1:n.11518T>A
|
|
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XM_011543675.1:c.11502T>A
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XP_011541977.1:p.Asp3834Glu
|
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XM_011543676.1:c.11424T>A
|
XP_011541978.1:p.Asp3808Glu
|
|
XM_011543677.1:c.8808T>A
|
XP_011541979.1:p.Asp2936Glu
|
|
XM_011543678.1:c.11505T>A
|
XP_011541980.1:p.Asp3835Glu
|
|
NM_032119.4:c.11505T>A
MANE Select
|
NP_115495.3:p.Asp3835Glu
|
|
XM_017009963.2:c.11526T>A
|
XP_016865452.1:p.Asp3842Glu
|
|
XM_017009964.2:c.11523T>A
|
XP_016865453.1:p.Asp3841Glu
|
|
XM_017009965.1:c.11523T>A
|
XP_016865454.1:p.Asp3841Glu
|
|
XM_017009966.2:c.11445T>A
|
XP_016865455.1:p.Asp3815Glu
|
|
XM_017009967.1:c.11430T>A
|
XP_016865456.1:p.Asp3810Glu
|
|
XM_017009968.2:c.11526T>A
|
XP_016865457.1:p.Asp3842Glu
|
|
XM_017009969.2:c.11526T>A
|
XP_016865458.1:p.Asp3842Glu
|
|
XM_017009970.2:c.11526T>A
|
XP_016865459.1:p.Asp3842Glu
|
|
XM_017009971.2:c.11526T>A
|
XP_016865460.1:p.Asp3842Glu
|
|
XM_017009972.1:c.4644T>A
|
XP_016865461.1:p.Asp1548Glu
|
|
XM_017009973.1:c.4623T>A
|
XP_016865462.1:p.Asp1541Glu
|
|
NR_003149.2:n.11521T>A
|
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