ENST00000559133.6:c.*1067T>A
|
ENSP00000453958.2:n.*1067T>A
|
|
ENST00000674301.2:c.*1772T>A
|
ENSP00000501333.2:n.*1772T>A
|
|
ENST00000682158.1:n.1640T>A
|
|
|
ENST00000682170.1:n.2440T>A
|
|
|
ENST00000682767.1:n.1556T>A
|
|
|
ENST00000316623.10:c.8259T>A
MANE Select
|
ENSP00000325527.5:p.Leu2753=
|
|
ENST00000674301.1:c.3425T>A
|
ENSP00000501333.1:n.3425T>A
|
|
ENST00000316623.9:c.8259T>A
|
ENSP00000325527.5:p.Leu2753=
|
|
ENST00000559133.5:c.3628T>A
|
|
|
ENST00000561429.1:n.514T>A
|
|
|
NM_000138.4:c.8259T>A , LRG_778t1:c.8259T>A
|
NP_000129.3:p.Leu2753=
|
|
NM_000138.5:c.8259T>A
MANE Select
|
NP_000129.3:p.Leu2753=
|
|