ENST00000405460.9:c.11384C>A
MANE Select
|
ENSP00000384582.2:p.Thr3795Asn
|
|
ENST00000425867.3:c.515C>A
|
ENSP00000392618.3:p.Thr172Asn
|
|
ENST00000639431.1:c.265+78780C>A
|
ENSP00000491057.1:n.265+78780C>A
|
|
ENST00000640374.1:n.4528C>A
|
|
|
ENST00000640464.1:n.1803C>A
|
|
|
ENST00000405460.6:c.11384C>A
|
ENSP00000384582.2:p.Thr3795Asn
|
|
ENST00000509621.1:c.4081C>A
|
|
|
NM_032119.3:c.11384C>A
|
NP_115495.3:p.Thr3795Asn
|
|
NR_003149.1:n.11397C>A
|
|
|
XM_011543675.1:c.11381C>A
|
XP_011541977.1:p.Thr3794Asn
|
|
XM_011543676.1:c.11303C>A
|
XP_011541978.1:p.Thr3768Asn
|
|
XM_011543677.1:c.8687C>A
|
XP_011541979.1:p.Thr2896Asn
|
|
XM_011543678.1:c.11384C>A
|
XP_011541980.1:p.Thr3795Asn
|
|
NM_032119.4:c.11384C>A
MANE Select
|
NP_115495.3:p.Thr3795Asn
|
|
XM_017009963.2:c.11405C>A
|
XP_016865452.1:p.Thr3802Asn
|
|
XM_017009964.2:c.11402C>A
|
XP_016865453.1:p.Thr3801Asn
|
|
XM_017009965.1:c.11402C>A
|
XP_016865454.1:p.Thr3801Asn
|
|
XM_017009966.2:c.11324C>A
|
XP_016865455.1:p.Thr3775Asn
|
|
XM_017009967.1:c.11309C>A
|
XP_016865456.1:p.Thr3770Asn
|
|
XM_017009968.2:c.11405C>A
|
XP_016865457.1:p.Thr3802Asn
|
|
XM_017009969.2:c.11405C>A
|
XP_016865458.1:p.Thr3802Asn
|
|
XM_017009970.2:c.11405C>A
|
XP_016865459.1:p.Thr3802Asn
|
|
XM_017009971.2:c.11405C>A
|
XP_016865460.1:p.Thr3802Asn
|
|
XM_017009972.1:c.4523C>A
|
XP_016865461.1:p.Thr1508Asn
|
|
XM_017009973.1:c.4502C>A
|
XP_016865462.1:p.Thr1501Asn
|
|
NR_003149.2:n.11400C>A
|
|
|