ENST00000326828.6:c.567G>C
MANE Select
|
ENSP00000315602.5:p.Leu189=
|
|
ENST00000326828.5:c.567G>C
|
ENSP00000315602.5:p.Leu189=
|
|
ENST00000348639.7:c.567G>C
|
ENSP00000267951.4:p.Leu189=
|
|
ENST00000558903.1:n.274G>C
|
|
|
ENST00000559658.5:c.567G>C
|
ENSP00000452896.1:p.Leu189=
|
|
NM_000743.4:c.567G>C
|
NP_000734.2:p.Leu189=
|
|
NM_001166694.1:c.567G>C
|
NP_001160166.1:p.Leu189=
|
|
NR_046313.1:n.1068G>C
|
|
|
XM_006720382.1:c.366G>C
|
XP_006720445.1:p.Leu122=
|
|
XM_011521173.1:c.486G>C
|
XP_011519475.1:p.Leu162=
|
|
XM_006720382.3:c.366G>C
|
XP_006720445.1:p.Leu122=
|
|
NM_000743.5:c.567G>C
MANE Select
|
NP_000734.2:p.Leu189=
|
|
NM_001166694.2:c.567G>C
|
NP_001160166.1:p.Leu189=
|
|
NR_046313.2:n.769G>C
|
|
|