|
NM_052813.5:c.424G=
MANE Select
|
NP_434700.2:p.Asp142=
|
|
ENST00000371732.10:c.424G=
MANE Select
|
ENSP00000360797.5:p.Asp142=
|
|
NM_052813.4:c.424G= , LRG_178t1:c.424G=
|
NP_434700.2:p.Asp142=
|
|
NM_052814.3:c.424G=
|
NP_434701.1:p.Asp142=
|
|
NM_052814.4:c.424G=
|
NP_434701.1:p.Asp142=
|
|
ENST00000371732.9:c.424G=
|
ENSP00000360797.5:p.Asp142=
|
|
ENST00000371734.7:c.424G=
|
ENSP00000360799.3:p.Asp142=
|
|
ENST00000481053.5:n.553G=
|
|
|
ENST00000489932.2:c.424G=
|
ENSP00000451368.1:p.Asp142=
|
|
ENST00000556340.1:n.555G=
|
|
|
ENST00000641290.1:c.112G=
|
ENSP00000493113.1:p.Asp38=
|
|
ENST00000641290.2:n.429G=
|
|
|
ENST00000695905.1:n.552G=
|
|
|
ENST00000695906.1:n.552G=
|
|
|
ENST00000695908.1:n.543G=
|
|
|
ENST00000696169.1:c.424G=
|
ENSP00000512460.1:p.Asp142=
|