ENST00000559133.6:c.*1157T>C
|
ENSP00000453958.2:n.*1157T>C
|
|
ENST00000674301.2:c.*1862T>C
|
ENSP00000501333.2:n.*1862T>C
|
|
ENST00000682158.1:n.1730T>C
|
|
|
ENST00000682170.1:n.2530T>C
|
|
|
ENST00000682767.1:n.1646T>C
|
|
|
ENST00000316623.10:c.8349T>C
MANE Select
|
ENSP00000325527.5:p.Ala2783=
|
|
ENST00000674301.1:c.3515T>C
|
ENSP00000501333.1:n.3515T>C
|
|
ENST00000316623.9:c.8349T>C
|
ENSP00000325527.5:p.Ala2783=
|
|
ENST00000559133.5:c.3718T>C
|
|
|
ENST00000561429.1:n.604T>C
|
|
|
NM_000138.4:c.8349T>C , LRG_778t1:c.8349T>C
|
NP_000129.3:p.Ala2783=
|
|
NM_000138.5:c.8349T>C
MANE Select
|
NP_000129.3:p.Ala2783=
|
|