ENST00000405460.9:c.9175A>T
MANE Select
|
ENSP00000384582.2:p.Asn3059Tyr
|
|
ENST00000639431.1:c.265+36210A>T
|
ENSP00000491057.1:n.265+36210A>T
|
|
ENST00000639473.1:n.4634A>T
|
|
|
ENST00000640012.1:c.2982A>T
|
|
|
ENST00000640374.1:n.2319A>T
|
|
|
ENST00000640779.1:c.3904A>T
|
|
|
ENST00000405460.6:c.9175A>T
|
ENSP00000384582.2:p.Asn3059Tyr
|
|
ENST00000509621.1:c.1872A>T
|
|
|
NM_032119.3:c.9175A>T
|
NP_115495.3:p.Asn3059Tyr
|
|
NR_003149.1:n.9188A>T
|
|
|
XM_011543675.1:c.9172A>T
|
XP_011541977.1:p.Asn3058Tyr
|
|
XM_011543676.1:c.9094A>T
|
XP_011541978.1:p.Asn3032Tyr
|
|
XM_011543677.1:c.6478A>T
|
XP_011541979.1:p.Asn2160Tyr
|
|
XM_011543678.1:c.9175A>T
|
XP_011541980.1:p.Asn3059Tyr
|
|
XM_011543679.1:c.9175A>T
|
XP_011541981.1:p.Asn3059Tyr
|
|
XR_948560.1:n.437-10T>A
|
|
|
NM_032119.4:c.9175A>T
MANE Select
|
NP_115495.3:p.Asn3059Tyr
|
|
XM_017009963.2:c.9196A>T
|
XP_016865452.1:p.Asn3066Tyr
|
|
XM_017009964.2:c.9193A>T
|
XP_016865453.1:p.Asn3065Tyr
|
|
XM_017009965.1:c.9193A>T
|
XP_016865454.1:p.Asn3065Tyr
|
|
XM_017009966.2:c.9115A>T
|
XP_016865455.1:p.Asn3039Tyr
|
|
XM_017009967.1:c.9100A>T
|
XP_016865456.1:p.Asn3034Tyr
|
|
XM_017009968.2:c.9196A>T
|
XP_016865457.1:p.Asn3066Tyr
|
|
XM_017009969.2:c.9196A>T
|
XP_016865458.1:p.Asn3066Tyr
|
|
XM_017009970.2:c.9196A>T
|
XP_016865459.1:p.Asn3066Tyr
|
|
XM_017009971.2:c.9196A>T
|
XP_016865460.1:p.Asn3066Tyr
|
|
XM_017009972.1:c.2314A>T
|
XP_016865461.1:p.Asn772Tyr
|
|
XM_017009973.1:c.2293A>T
|
XP_016865462.1:p.Asn765Tyr
|
|
XM_017009974.2:c.9196A>T
|
XP_016865463.1:p.Asn3066Tyr
|
|
NR_003149.2:n.9191A>T
|
|
|