ENST00000682114.1:c.419T>A
|
ENSP00000507245.1:p.Leu140Ter
|
|
ENST00000682478.1:n.609T>A
|
|
|
ENST00000683576.1:n.609T>A
|
|
|
ENST00000683627.1:c.419T>A
|
ENSP00000507533.1:p.Leu140Ter
|
|
ENST00000684082.1:c.376T>A
|
ENSP00000508266.1:n.376T>A
|
|
ENST00000684633.1:n.391T>A
|
|
|
ENST00000684678.1:c.415T>A
|
ENSP00000507059.1:n.415T>A
|
|
ENST00000369842.9:c.419T>A
MANE Select
|
ENSP00000358857.4:p.Leu140Ter
|
|
ENST00000369835.3:c.314T>A
|
ENSP00000358850.3:p.Leu105Ter
|
|
ENST00000369842.8:c.419T>A
|
ENSP00000358857.4:p.Leu140Ter
|
|
ENST00000428228.5:c.*324T>A
|
ENSP00000401081.1:n.*324T>A
|
|
ENST00000468294.5:n.379T>A
|
|
|
ENST00000471965.1:n.208T>A
|
|
|
ENST00000485261.1:n.609T>A
|
|
|
ENST00000486738.5:n.777T>A
|
|
|
ENST00000492448.1:n.402T>A
|
|
|
NM_000117.2:c.419T>A , LRG_745t1:c.419T>A
|
NP_000108.1:p.Leu140Ter
|
|
XM_024452349.1:c.425T>A
|
XP_024308117.1:p.Leu142Ter
|
|
NM_000117.3:c.419T>A
MANE Select
|
NP_000108.1:p.Leu140Ter
|
|