ENST00000405460.9:c.12127A>T
MANE Select
|
ENSP00000384582.2:p.Ile4043Phe
|
|
ENST00000425867.3:c.1081A>T
|
ENSP00000392618.3:p.Ile361Phe
|
|
ENST00000639431.1:c.265+87102A>T
|
ENSP00000491057.1:n.265+87102A>T
|
|
ENST00000640464.1:n.2546A>T
|
|
|
ENST00000640729.1:n.704A>T
|
|
|
ENST00000405460.6:c.12127A>T
|
ENSP00000384582.2:p.Ile4043Phe
|
|
NM_032119.3:c.12127A>T
|
NP_115495.3:p.Ile4043Phe
|
|
NR_003149.1:n.12140A>T
|
|
|
XM_011543675.1:c.12124A>T
|
XP_011541977.1:p.Ile4042Phe
|
|
XM_011543676.1:c.12046A>T
|
XP_011541978.1:p.Ile4016Phe
|
|
XM_011543677.1:c.9430A>T
|
XP_011541979.1:p.Ile3144Phe
|
|
XM_011543678.1:c.12127A>T
|
XP_011541980.1:p.Ile4043Phe
|
|
NM_032119.4:c.12127A>T
MANE Select
|
NP_115495.3:p.Ile4043Phe
|
|
XM_017009963.2:c.12148A>T
|
XP_016865452.1:p.Ile4050Phe
|
|
XM_017009964.2:c.12145A>T
|
XP_016865453.1:p.Ile4049Phe
|
|
XM_017009965.1:c.12145A>T
|
XP_016865454.1:p.Ile4049Phe
|
|
XM_017009966.2:c.12067A>T
|
XP_016865455.1:p.Ile4023Phe
|
|
XM_017009967.1:c.12052A>T
|
XP_016865456.1:p.Ile4018Phe
|
|
XM_017009968.2:c.12148A>T
|
XP_016865457.1:p.Ile4050Phe
|
|
XM_017009969.2:c.12148A>T
|
XP_016865458.1:p.Ile4050Phe
|
|
XM_017009970.2:c.12148A>T
|
XP_016865459.1:p.Ile4050Phe
|
|
XM_017009971.2:c.12148A>T
|
XP_016865460.1:p.Ile4050Phe
|
|
XM_017009972.1:c.5266A>T
|
XP_016865461.1:p.Ile1756Phe
|
|
XM_017009973.1:c.5245A>T
|
XP_016865462.1:p.Ile1749Phe
|
|
NR_003149.2:n.12143A>T
|
|
|