|
NM_032119.4:c.15244C>T
MANE Select
|
NP_115495.3:p.Gln5082Ter
|
|
ENST00000405460.9:c.15244C>T
MANE Select
|
ENSP00000384582.2:p.Gln5082Ter
|
|
NM_032119.3:c.15244C>T
|
NP_115495.3:p.Gln5082Ter
|
|
NR_003149.1:n.15257C>T
|
|
|
NR_003149.2:n.15260C>T
|
|
|
ENST00000405460.6:c.15244C>T
|
ENSP00000384582.2:p.Gln5082Ter
|
|
ENST00000425867.2:c.2227C>T
|
ENSP00000392618.2:p.Gln743Ter
|
|
ENST00000425867.3:c.4198C>T
|
ENSP00000392618.3:p.Gln1400Ter
|
|
ENST00000638510.1:n.2511C>T
|
|
|
ENST00000639431.1:c.265+134295C>T
|
ENSP00000491057.1:n.265+134295C>T
|
|
ENST00000640407.1:c.1654C>T
|
ENSP00000491425.1:p.Gln552Ter
|
|
XM_011543675.1:c.15241C>T
|
XP_011541977.1:p.Gln5081Ter
|
|
XM_011543676.1:c.15163C>T
|
XP_011541978.1:p.Gln5055Ter
|
|
XM_011543677.1:c.12547C>T
|
XP_011541979.1:p.Gln4183Ter
|
|
XM_017009963.2:c.15265C>T
|
XP_016865452.1:p.Gln5089Ter
|
|
XM_017009964.2:c.15262C>T
|
XP_016865453.1:p.Gln5088Ter
|
|
XM_017009965.1:c.15262C>T
|
XP_016865454.1:p.Gln5088Ter
|
|
XM_017009966.2:c.15184C>T
|
XP_016865455.1:p.Gln5062Ter
|
|
XM_017009967.1:c.15169C>T
|
XP_016865456.1:p.Gln5057Ter
|
|
XM_017009968.2:c.15085C>T
|
XP_016865457.1:p.Gln5029Ter
|
|
XM_017009969.2:c.15265C>T
|
XP_016865458.1:p.Gln5089Ter
|
|
XM_017009971.2:c.*198C>T
|
XP_016865460.1:n.*198C>T
|
|
XM_017009972.1:c.8383C>T
|
XP_016865461.1:p.Gln2795Ter
|
|
XM_017009973.1:c.8362C>T
|
XP_016865462.1:p.Gln2788Ter
|