ENST00000584880.6:c.*416T>A
|
ENSP00000464347.2:n.*416T>A
|
|
ENST00000703608.1:c.*736T>A
|
ENSP00000515392.1:n.*736T>A
|
|
ENST00000703609.1:c.1138T>A
|
ENSP00000515393.1:p.Ter380Arg
|
|
ENST00000703610.1:c.*496T>A
|
ENSP00000515394.1:n.*496T>A
|
|
ENST00000310144.11:c.1219T>A
MANE Select
|
ENSP00000310572.6:p.Ter407Arg
|
|
ENST00000310144.10:c.1219T>A
|
ENSP00000310572.6:p.Ter407Arg
|
|
ENST00000375812.8:c.1195T>A
|
ENSP00000364970.4:p.Ter399Arg
|
|
ENST00000578570.5:n.1629T>A
|
|
|
ENST00000579147.5:n.2534T>A
|
|
|
ENST00000580864.5:c.1195T>A
|
ENSP00000462495.1:p.Ter399Arg
|
|
ENST00000581882.5:c.1195T>A
|
ENSP00000463938.1:p.Ter399Arg
|
|
ENST00000584657.1:n.524T>A
|
|
|
ENST00000585242.5:c.*990T>A
|
ENSP00000463107.1:n.*990T>A
|
|
NM_001199163.1:c.1195T>A
|
NP_001186092.1:p.Ter399Arg
|
|
NM_002805.5:c.1219T>A
|
NP_002796.4:p.Ter407Arg
|
|
XM_006721980.1:c.1219T>A
|
XP_006722043.1:p.Ter407Arg
|
|
XR_934508.1:n.1308T>A
|
|
|
XM_024450840.1:c.1300T>A
|
XP_024306608.1:p.Ter434Arg
|
|
XM_024450841.1:c.1276T>A
|
XP_024306609.1:p.Ter426Arg
|
|
XR_934508.2:n.1295T>A
|
|
|
NM_002805.6:c.1219T>A
MANE Select
|
NP_002796.4:p.Ter407Arg
|
|
NM_001199163.2:c.1195T>A
|
NP_001186092.1:p.Ter399Arg
|
|