ENST00000559133.6:c.*1243T=
|
ENSP00000453958.2:n.*1243T=
|
|
ENST00000674301.2:c.*1948T=
|
ENSP00000501333.2:n.*1948T=
|
|
ENST00000682158.1:n.1816T=
|
|
|
ENST00000682170.1:n.2616T=
|
|
|
ENST00000682767.1:n.1732T=
|
|
|
ENST00000316623.10:c.8435T=
MANE Select
|
ENSP00000325527.5:p.Ile2812=
|
|
ENST00000674301.1:c.3601T=
|
ENSP00000501333.1:n.3601T=
|
|
ENST00000316623.9:c.8435T=
|
ENSP00000325527.5:p.Ile2812=
|
|
ENST00000559133.5:c.3804T=
|
|
|
NM_000138.4:c.8435T= , LRG_778t1:c.8435T=
|
NP_000129.3:p.Ile2812=
|
|
NM_000138.5:c.8435T=
MANE Select
|
NP_000129.3:p.Ile2812=
|
|