ENST00000559133.6:c.*697A>T
|
ENSP00000453958.2:n.*697A>T
|
|
ENST00000674301.2:c.*1402A>T
|
ENSP00000501333.2:n.*1402A>T
|
|
ENST00000682158.1:n.1270A>T
|
|
|
ENST00000682170.1:n.2070A>T
|
|
|
ENST00000682767.1:n.1186A>T
|
|
|
ENST00000316623.10:c.7889A>T
MANE Select
|
ENSP00000325527.5:p.Lys2630Met
|
|
ENST00000674301.1:c.3055A>T
|
ENSP00000501333.1:n.3055A>T
|
|
ENST00000316623.9:c.7889A>T
|
ENSP00000325527.5:p.Lys2630Met
|
|
ENST00000559133.5:c.3258A>T
|
|
|
ENST00000561429.1:n.144A>T
|
|
|
NM_000138.4:c.7889A>T , LRG_778t1:c.7889A>T
|
NP_000129.3:p.Lys2630Met
|
|
NM_000138.5:c.7889A>T
MANE Select
|
NP_000129.3:p.Lys2630Met
|
|