ENST00000559133.6:c.*1142A>T
|
ENSP00000453958.2:n.*1142A>T
|
|
ENST00000674301.2:c.*1847A>T
|
ENSP00000501333.2:n.*1847A>T
|
|
ENST00000682158.1:n.1715A>T
|
|
|
ENST00000682170.1:n.2515A>T
|
|
|
ENST00000682767.1:n.1631A>T
|
|
|
ENST00000316623.10:c.8334A>T
MANE Select
|
ENSP00000325527.5:p.Leu2778=
|
|
ENST00000674301.1:c.3500A>T
|
ENSP00000501333.1:n.3500A>T
|
|
ENST00000316623.9:c.8334A>T
|
ENSP00000325527.5:p.Leu2778=
|
|
ENST00000559133.5:c.3703A>T
|
|
|
ENST00000561429.1:n.589A>T
|
|
|
NM_000138.4:c.8334A>T , LRG_778t1:c.8334A>T
|
NP_000129.3:p.Leu2778=
|
|
NM_000138.5:c.8334A>T
MANE Select
|
NP_000129.3:p.Leu2778=
|
|