ENST00000405460.9:c.11491A=
MANE Select
|
ENSP00000384582.2:p.Thr3831=
|
|
ENST00000425867.3:c.622A=
|
ENSP00000392618.3:p.Thr208=
|
|
ENST00000639431.1:c.265+78887A=
|
ENSP00000491057.1:n.265+78887A=
|
|
ENST00000640374.1:n.4635A=
|
|
|
ENST00000640464.1:n.1910A=
|
|
|
ENST00000405460.6:c.11491A=
|
ENSP00000384582.2:p.Thr3831=
|
|
ENST00000509621.1:c.4188A=
|
|
|
NM_032119.3:c.11491A=
|
NP_115495.3:p.Thr3831=
|
|
NR_003149.1:n.11504A=
|
|
|
XM_011543675.1:c.11488A=
|
XP_011541977.1:p.Thr3830=
|
|
XM_011543676.1:c.11410A=
|
XP_011541978.1:p.Thr3804=
|
|
XM_011543677.1:c.8794A=
|
XP_011541979.1:p.Thr2932=
|
|
XM_011543678.1:c.11491A=
|
XP_011541980.1:p.Thr3831=
|
|
NM_032119.4:c.11491A=
MANE Select
|
NP_115495.3:p.Thr3831=
|
|
XM_017009963.2:c.11512A=
|
XP_016865452.1:p.Thr3838=
|
|
XM_017009964.2:c.11509A=
|
XP_016865453.1:p.Thr3837=
|
|
XM_017009965.1:c.11509A=
|
XP_016865454.1:p.Thr3837=
|
|
XM_017009966.2:c.11431A=
|
XP_016865455.1:p.Thr3811=
|
|
XM_017009967.1:c.11416A=
|
XP_016865456.1:p.Thr3806=
|
|
XM_017009968.2:c.11512A=
|
XP_016865457.1:p.Thr3838=
|
|
XM_017009969.2:c.11512A=
|
XP_016865458.1:p.Thr3838=
|
|
XM_017009970.2:c.11512A=
|
XP_016865459.1:p.Thr3838=
|
|
XM_017009971.2:c.11512A=
|
XP_016865460.1:p.Thr3838=
|
|
XM_017009972.1:c.4630A=
|
XP_016865461.1:p.Thr1544=
|
|
XM_017009973.1:c.4609A=
|
XP_016865462.1:p.Thr1537=
|
|
NR_003149.2:n.11507A=
|
|
|