ENST00000405460.9:c.11533del
MANE Select
|
ENSP00000384582.2:p.Met3845Ter
|
|
ENST00000425867.3:c.664del
|
ENSP00000392618.3:p.Met222Ter
|
|
ENST00000639431.1:c.265+78929del
|
ENSP00000491057.1:n.265+78929del
|
|
ENST00000640374.1:n.4677del
|
|
|
ENST00000640464.1:n.1952del
|
|
|
ENST00000405460.6:c.11533del
|
ENSP00000384582.2:p.Met3845Ter
|
|
ENST00000509621.1:c.4230del
|
|
|
NM_032119.3:c.11533del
|
NP_115495.3:p.Met3845Ter
|
|
NR_003149.1:n.11546del
|
|
|
XM_011543675.1:c.11530del
|
XP_011541977.1:p.Met3844Ter
|
|
XM_011543676.1:c.11452del
|
XP_011541978.1:p.Met3818Ter
|
|
XM_011543677.1:c.8836del
|
XP_011541979.1:p.Met2946Ter
|
|
XM_011543678.1:c.11533del
|
XP_011541980.1:p.Met3845Ter
|
|
NM_032119.4:c.11533del
MANE Select
|
NP_115495.3:p.Met3845Ter
|
|
XM_017009963.2:c.11554del
|
XP_016865452.1:p.Met3852Ter
|
|
XM_017009964.2:c.11551del
|
XP_016865453.1:p.Met3851Ter
|
|
XM_017009965.1:c.11551del
|
XP_016865454.1:p.Met3851Ter
|
|
XM_017009966.2:c.11473del
|
XP_016865455.1:p.Met3825Ter
|
|
XM_017009967.1:c.11458del
|
XP_016865456.1:p.Met3820Ter
|
|
XM_017009968.2:c.11554del
|
XP_016865457.1:p.Met3852Ter
|
|
XM_017009969.2:c.11554del
|
XP_016865458.1:p.Met3852Ter
|
|
XM_017009970.2:c.11554del
|
XP_016865459.1:p.Met3852Ter
|
|
XM_017009971.2:c.11554del
|
XP_016865460.1:p.Met3852Ter
|
|
XM_017009972.1:c.4672del
|
XP_016865461.1:p.Met1558Ter
|
|
XM_017009973.1:c.4651del
|
XP_016865462.1:p.Met1551Ter
|
|
NR_003149.2:n.11549del
|
|
|