|
NM_032119.4:c.11687T>A
MANE Select
|
NP_115495.3:p.Met3896Lys
|
|
ENST00000405460.9:c.11687T>A
MANE Select
|
ENSP00000384582.2:p.Met3896Lys
|
|
NM_032119.3:c.11687T>A
|
NP_115495.3:p.Met3896Lys
|
|
NR_003149.1:n.11700T>A
|
|
|
NR_003149.2:n.11703T>A
|
|
|
ENST00000405460.6:c.11687T>A
|
ENSP00000384582.2:p.Met3896Lys
|
|
ENST00000425867.3:c.712-419T>A
|
ENSP00000392618.3:n.712-419T>A
|
|
ENST00000509621.1:c.4384T>A
|
|
|
ENST00000639431.1:c.265+80351T>A
|
ENSP00000491057.1:n.265+80351T>A
|
|
ENST00000640374.1:n.4725-419T>A
|
|
|
ENST00000640464.1:n.2106T>A
|
|
|
XM_011543675.1:c.11684T>A
|
XP_011541977.1:p.Met3895Lys
|
|
XM_011543676.1:c.11606T>A
|
XP_011541978.1:p.Met3869Lys
|
|
XM_011543677.1:c.8990T>A
|
XP_011541979.1:p.Met2997Lys
|
|
XM_011543678.1:c.11687T>A
|
XP_011541980.1:p.Met3896Lys
|
|
XM_017009963.2:c.11708T>A
|
XP_016865452.1:p.Met3903Lys
|
|
XM_017009964.2:c.11705T>A
|
XP_016865453.1:p.Met3902Lys
|
|
XM_017009965.1:c.11705T>A
|
XP_016865454.1:p.Met3902Lys
|
|
XM_017009966.2:c.11627T>A
|
XP_016865455.1:p.Met3876Lys
|
|
XM_017009967.1:c.11612T>A
|
XP_016865456.1:p.Met3871Lys
|
|
XM_017009968.2:c.11708T>A
|
XP_016865457.1:p.Met3903Lys
|
|
XM_017009969.2:c.11708T>A
|
XP_016865458.1:p.Met3903Lys
|
|
XM_017009970.2:c.11708T>A
|
XP_016865459.1:p.Met3903Lys
|
|
XM_017009971.2:c.11708T>A
|
XP_016865460.1:p.Met3903Lys
|
|
XM_017009972.1:c.4826T>A
|
XP_016865461.1:p.Met1609Lys
|
|
XM_017009973.1:c.4805T>A
|
XP_016865462.1:p.Met1602Lys
|