ENST00000405460.9:c.12143C>G
MANE Select
|
ENSP00000384582.2:p.Ser4048Ter
|
|
ENST00000425867.3:c.1097C>G
|
ENSP00000392618.3:p.Ser366Ter
|
|
ENST00000639431.1:c.265+87118C>G
|
ENSP00000491057.1:n.265+87118C>G
|
|
ENST00000640464.1:n.2562C>G
|
|
|
ENST00000640729.1:n.720C>G
|
|
|
ENST00000405460.6:c.12143C>G
|
ENSP00000384582.2:p.Ser4048Ter
|
|
NM_032119.3:c.12143C>G
|
NP_115495.3:p.Ser4048Ter
|
|
NR_003149.1:n.12156C>G
|
|
|
XM_011543675.1:c.12140C>G
|
XP_011541977.1:p.Ser4047Ter
|
|
XM_011543676.1:c.12062C>G
|
XP_011541978.1:p.Ser4021Ter
|
|
XM_011543677.1:c.9446C>G
|
XP_011541979.1:p.Ser3149Ter
|
|
XM_011543678.1:c.12143C>G
|
XP_011541980.1:p.Ser4048Ter
|
|
NM_032119.4:c.12143C>G
MANE Select
|
NP_115495.3:p.Ser4048Ter
|
|
XM_017009963.2:c.12164C>G
|
XP_016865452.1:p.Ser4055Ter
|
|
XM_017009964.2:c.12161C>G
|
XP_016865453.1:p.Ser4054Ter
|
|
XM_017009965.1:c.12161C>G
|
XP_016865454.1:p.Ser4054Ter
|
|
XM_017009966.2:c.12083C>G
|
XP_016865455.1:p.Ser4028Ter
|
|
XM_017009967.1:c.12068C>G
|
XP_016865456.1:p.Ser4023Ter
|
|
XM_017009968.2:c.12164C>G
|
XP_016865457.1:p.Ser4055Ter
|
|
XM_017009969.2:c.12164C>G
|
XP_016865458.1:p.Ser4055Ter
|
|
XM_017009970.2:c.12164C>G
|
XP_016865459.1:p.Ser4055Ter
|
|
XM_017009971.2:c.12164C>G
|
XP_016865460.1:p.Ser4055Ter
|
|
XM_017009972.1:c.5282C>G
|
XP_016865461.1:p.Ser1761Ter
|
|
XM_017009973.1:c.5261C>G
|
XP_016865462.1:p.Ser1754Ter
|
|
NR_003149.2:n.12159C>G
|
|
|