ENST00000405460.9:c.9180A>G
MANE Select
|
ENSP00000384582.2:p.Thr3060=
|
|
ENST00000639431.1:c.265+36215A>G
|
ENSP00000491057.1:n.265+36215A>G
|
|
ENST00000639473.1:n.4639A>G
|
|
|
ENST00000640012.1:c.2987A>G
|
|
|
ENST00000640374.1:n.2324A>G
|
|
|
ENST00000640779.1:c.3909A>G
|
|
|
ENST00000405460.6:c.9180A>G
|
ENSP00000384582.2:p.Thr3060=
|
|
ENST00000509621.1:c.1877A>G
|
|
|
NM_032119.3:c.9180A>G
|
NP_115495.3:p.Thr3060=
|
|
NR_003149.1:n.9193A>G
|
|
|
XM_011543675.1:c.9177A>G
|
XP_011541977.1:p.Thr3059=
|
|
XM_011543676.1:c.9099A>G
|
XP_011541978.1:p.Thr3033=
|
|
XM_011543677.1:c.6483A>G
|
XP_011541979.1:p.Thr2161=
|
|
XM_011543678.1:c.9180A>G
|
XP_011541980.1:p.Thr3060=
|
|
XM_011543679.1:c.9180A>G
|
XP_011541981.1:p.Thr3060=
|
|
XR_948560.1:n.437-15T>C
|
|
|
NM_032119.4:c.9180A>G
MANE Select
|
NP_115495.3:p.Thr3060=
|
|
XM_017009963.2:c.9201A>G
|
XP_016865452.1:p.Thr3067=
|
|
XM_017009964.2:c.9198A>G
|
XP_016865453.1:p.Thr3066=
|
|
XM_017009965.1:c.9198A>G
|
XP_016865454.1:p.Thr3066=
|
|
XM_017009966.2:c.9120A>G
|
XP_016865455.1:p.Thr3040=
|
|
XM_017009967.1:c.9105A>G
|
XP_016865456.1:p.Thr3035=
|
|
XM_017009968.2:c.9201A>G
|
XP_016865457.1:p.Thr3067=
|
|
XM_017009969.2:c.9201A>G
|
XP_016865458.1:p.Thr3067=
|
|
XM_017009970.2:c.9201A>G
|
XP_016865459.1:p.Thr3067=
|
|
XM_017009971.2:c.9201A>G
|
XP_016865460.1:p.Thr3067=
|
|
XM_017009972.1:c.2319A>G
|
XP_016865461.1:p.Thr773=
|
|
XM_017009973.1:c.2298A>G
|
XP_016865462.1:p.Thr766=
|
|
XM_017009974.2:c.9201A>G
|
XP_016865463.1:p.Thr3067=
|
|
NR_003149.2:n.9196A>G
|
|
|