ENST00000559133.6:c.*1064T>G
|
ENSP00000453958.2:n.*1064T>G
|
|
ENST00000674301.2:c.*1769T>G
|
ENSP00000501333.2:n.*1769T>G
|
|
ENST00000682158.1:n.1637T>G
|
|
|
ENST00000682170.1:n.2437T>G
|
|
|
ENST00000682767.1:n.1553T>G
|
|
|
ENST00000316623.10:c.8256T>G
MANE Select
|
ENSP00000325527.5:p.Ser2752Arg
|
|
ENST00000674301.1:c.3422T>G
|
ENSP00000501333.1:n.3422T>G
|
|
ENST00000316623.9:c.8256T>G
|
ENSP00000325527.5:p.Ser2752Arg
|
|
ENST00000559133.5:c.3625T>G
|
|
|
ENST00000561429.1:n.511T>G
|
|
|
NM_000138.4:c.8256T>G , LRG_778t1:c.8256T>G
|
NP_000129.3:p.Ser2752Arg
|
|
NM_000138.5:c.8256T>G
MANE Select
|
NP_000129.3:p.Ser2752Arg
|
|