ENST00000405460.9:c.12133G>T
MANE Select
|
ENSP00000384582.2:p.Glu4045Ter
|
|
ENST00000425867.3:c.1087G>T
|
ENSP00000392618.3:p.Glu363Ter
|
|
ENST00000639431.1:c.265+87108G>T
|
ENSP00000491057.1:n.265+87108G>T
|
|
ENST00000640464.1:n.2552G>T
|
|
|
ENST00000640729.1:n.710G>T
|
|
|
ENST00000405460.6:c.12133G>T
|
ENSP00000384582.2:p.Glu4045Ter
|
|
NM_032119.3:c.12133G>T
|
NP_115495.3:p.Glu4045Ter
|
|
NR_003149.1:n.12146G>T
|
|
|
XM_011543675.1:c.12130G>T
|
XP_011541977.1:p.Glu4044Ter
|
|
XM_011543676.1:c.12052G>T
|
XP_011541978.1:p.Glu4018Ter
|
|
XM_011543677.1:c.9436G>T
|
XP_011541979.1:p.Glu3146Ter
|
|
XM_011543678.1:c.12133G>T
|
XP_011541980.1:p.Glu4045Ter
|
|
NM_032119.4:c.12133G>T
MANE Select
|
NP_115495.3:p.Glu4045Ter
|
|
XM_017009963.2:c.12154G>T
|
XP_016865452.1:p.Glu4052Ter
|
|
XM_017009964.2:c.12151G>T
|
XP_016865453.1:p.Glu4051Ter
|
|
XM_017009965.1:c.12151G>T
|
XP_016865454.1:p.Glu4051Ter
|
|
XM_017009966.2:c.12073G>T
|
XP_016865455.1:p.Glu4025Ter
|
|
XM_017009967.1:c.12058G>T
|
XP_016865456.1:p.Glu4020Ter
|
|
XM_017009968.2:c.12154G>T
|
XP_016865457.1:p.Glu4052Ter
|
|
XM_017009969.2:c.12154G>T
|
XP_016865458.1:p.Glu4052Ter
|
|
XM_017009970.2:c.12154G>T
|
XP_016865459.1:p.Glu4052Ter
|
|
XM_017009971.2:c.12154G>T
|
XP_016865460.1:p.Glu4052Ter
|
|
XM_017009972.1:c.5272G>T
|
XP_016865461.1:p.Glu1758Ter
|
|
XM_017009973.1:c.5251G>T
|
XP_016865462.1:p.Glu1751Ter
|
|
NR_003149.2:n.12149G>T
|
|
|