ENST00000405460.9:c.12161C=
MANE Select
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ENSP00000384582.2:p.Ser4054=
|
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ENST00000425867.3:c.1115C=
|
ENSP00000392618.3:p.Ser372=
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|
ENST00000639431.1:c.265+87136C=
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ENSP00000491057.1:n.265+87136C=
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ENST00000640464.1:n.2580C=
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|
|
ENST00000640729.1:n.738C=
|
|
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ENST00000405460.6:c.12161C=
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ENSP00000384582.2:p.Ser4054=
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|
NM_032119.3:c.12161C=
|
NP_115495.3:p.Ser4054=
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NR_003149.1:n.12174C=
|
|
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XM_011543675.1:c.12158C=
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XP_011541977.1:p.Ser4053=
|
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XM_011543676.1:c.12080C=
|
XP_011541978.1:p.Ser4027=
|
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XM_011543677.1:c.9464C=
|
XP_011541979.1:p.Ser3155=
|
|
XM_011543678.1:c.12161C=
|
XP_011541980.1:p.Ser4054=
|
|
NM_032119.4:c.12161C=
MANE Select
|
NP_115495.3:p.Ser4054=
|
|
XM_017009963.2:c.12182C=
|
XP_016865452.1:p.Ser4061=
|
|
XM_017009964.2:c.12179C=
|
XP_016865453.1:p.Ser4060=
|
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XM_017009965.1:c.12179C=
|
XP_016865454.1:p.Ser4060=
|
|
XM_017009966.2:c.12101C=
|
XP_016865455.1:p.Ser4034=
|
|
XM_017009967.1:c.12086C=
|
XP_016865456.1:p.Ser4029=
|
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XM_017009968.2:c.12182C=
|
XP_016865457.1:p.Ser4061=
|
|
XM_017009969.2:c.12182C=
|
XP_016865458.1:p.Ser4061=
|
|
XM_017009970.2:c.12182C=
|
XP_016865459.1:p.Ser4061=
|
|
XM_017009971.2:c.12182C=
|
XP_016865460.1:p.Ser4061=
|
|
XM_017009972.1:c.5300C=
|
XP_016865461.1:p.Ser1767=
|
|
XM_017009973.1:c.5279C=
|
XP_016865462.1:p.Ser1760=
|
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NR_003149.2:n.12177C=
|
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