ENST00000559133.6:c.6996T>A
|
ENSP00000453958.2:p.Leu2332=
|
|
ENST00000674301.2:c.*447T>A
|
ENSP00000501333.2:n.*447T>A
|
|
ENST00000682170.1:n.605T>A
|
|
|
ENST00000682767.1:n.231T>A
|
|
|
ENST00000316623.10:c.6996T>A
MANE Select
|
ENSP00000325527.5:p.Leu2332=
|
|
ENST00000674301.1:c.2100T>A
|
ENSP00000501333.1:n.2100T>A
|
|
ENST00000316623.9:c.6996T>A
|
ENSP00000325527.5:p.Leu2332=
|
|
ENST00000559133.5:c.2303T>A
|
|
|
ENST00000560720.1:n.283T>A
|
|
|
NM_000138.4:c.6996T>A , LRG_778t1:c.6996T>A
|
NP_000129.3:p.Leu2332=
|
|
NM_000138.5:c.6996T>A
MANE Select
|
NP_000129.3:p.Leu2332=
|
|