|
NM_032119.4:c.12497C>G
MANE Select
|
NP_115495.3:p.Ser4166Ter
|
|
ENST00000405460.9:c.12497C>G
MANE Select
|
ENSP00000384582.2:p.Ser4166Ter
|
|
NM_032119.3:c.12497C>G
|
NP_115495.3:p.Ser4166Ter
|
|
NR_003149.1:n.12510C>G
|
|
|
NR_003149.2:n.12513C>G
|
|
|
ENST00000405460.6:c.12497C>G
|
ENSP00000384582.2:p.Ser4166Ter
|
|
ENST00000425867.3:c.1451C>G
|
ENSP00000392618.3:p.Ser484Ter
|
|
ENST00000639431.1:c.265+100337C>G
|
ENSP00000491057.1:n.265+100337C>G
|
|
ENST00000640464.1:n.2916C>G
|
|
|
ENST00000640729.1:n.1074C>G
|
|
|
XM_011543675.1:c.12494C>G
|
XP_011541977.1:p.Ser4165Ter
|
|
XM_011543676.1:c.12416C>G
|
XP_011541978.1:p.Ser4139Ter
|
|
XM_011543677.1:c.9800C>G
|
XP_011541979.1:p.Ser3267Ter
|
|
XM_011543678.1:c.12497C>G
|
XP_011541980.1:p.Ser4166Ter
|
|
XM_017009963.2:c.12518C>G
|
XP_016865452.1:p.Ser4173Ter
|
|
XM_017009964.2:c.12515C>G
|
XP_016865453.1:p.Ser4172Ter
|
|
XM_017009965.1:c.12515C>G
|
XP_016865454.1:p.Ser4172Ter
|
|
XM_017009966.2:c.12437C>G
|
XP_016865455.1:p.Ser4146Ter
|
|
XM_017009967.1:c.12422C>G
|
XP_016865456.1:p.Ser4141Ter
|
|
XM_017009968.2:c.12518C>G
|
XP_016865457.1:p.Ser4173Ter
|
|
XM_017009969.2:c.12518C>G
|
XP_016865458.1:p.Ser4173Ter
|
|
XM_017009970.2:c.12518C>G
|
XP_016865459.1:p.Ser4173Ter
|
|
XM_017009971.2:c.12518C>G
|
XP_016865460.1:p.Ser4173Ter
|
|
XM_017009972.1:c.5636C>G
|
XP_016865461.1:p.Ser1879Ter
|
|
XM_017009973.1:c.5615C>G
|
XP_016865462.1:p.Ser1872Ter
|