ENST00000405460.9:c.10938T>A
MANE Select
|
ENSP00000384582.2:p.Ser3646=
|
|
ENST00000425867.3:c.69T>A
|
ENSP00000392618.3:p.Ser23=
|
|
ENST00000639431.1:c.265+69550T>A
|
ENSP00000491057.1:n.265+69550T>A
|
|
ENST00000640374.1:n.4082T>A
|
|
|
ENST00000640464.1:n.1357T>A
|
|
|
ENST00000405460.6:c.10938T>A
|
ENSP00000384582.2:p.Ser3646=
|
|
ENST00000509621.1:c.3635T>A
|
|
|
NM_032119.3:c.10938T>A
|
NP_115495.3:p.Ser3646=
|
|
NR_003149.1:n.10951T>A
|
|
|
XM_011543675.1:c.10935T>A
|
XP_011541977.1:p.Ser3645=
|
|
XM_011543676.1:c.10857T>A
|
XP_011541978.1:p.Ser3619=
|
|
XM_011543677.1:c.8241T>A
|
XP_011541979.1:p.Ser2747=
|
|
XM_011543678.1:c.10938T>A
|
XP_011541980.1:p.Ser3646=
|
|
NM_032119.4:c.10938T>A
MANE Select
|
NP_115495.3:p.Ser3646=
|
|
XM_017009963.2:c.10959T>A
|
XP_016865452.1:p.Ser3653=
|
|
XM_017009964.2:c.10956T>A
|
XP_016865453.1:p.Ser3652=
|
|
XM_017009965.1:c.10956T>A
|
XP_016865454.1:p.Ser3652=
|
|
XM_017009966.2:c.10878T>A
|
XP_016865455.1:p.Ser3626=
|
|
XM_017009967.1:c.10863T>A
|
XP_016865456.1:p.Ser3621=
|
|
XM_017009968.2:c.10959T>A
|
XP_016865457.1:p.Ser3653=
|
|
XM_017009969.2:c.10959T>A
|
XP_016865458.1:p.Ser3653=
|
|
XM_017009970.2:c.10959T>A
|
XP_016865459.1:p.Ser3653=
|
|
XM_017009971.2:c.10959T>A
|
XP_016865460.1:p.Ser3653=
|
|
XM_017009972.1:c.4077T>A
|
XP_016865461.1:p.Ser1359=
|
|
XM_017009973.1:c.4056T>A
|
XP_016865462.1:p.Ser1352=
|
|
NR_003149.2:n.10954T>A
|
|
|