ENST00000356392.9:c.1197G=
MANE Select
|
ENSP00000348757.3:p.Leu399=
|
|
ENST00000356392.8:c.1197G=
|
ENSP00000348757.3:p.Leu399=
|
|
ENST00000586836.5:c.624G=
|
ENSP00000467429.1:p.Leu208=
|
|
ENST00000591179.5:c.1017G=
|
ENSP00000466800.1:p.Leu339=
|
|
ENST00000591345.5:c.*1116G=
|
ENSP00000467313.1:n.*1116G=
|
|
NM_001302453.1:c.1035G=
|
NP_001289382.1:p.Leu345=
|
|
NM_001302454.1:c.1017G=
|
NP_001289383.1:p.Leu339=
|
|
NM_145045.4:c.1197G=
|
NP_659482.3:p.Leu399=
|
|
XM_017026241.1:c.*91G=
|
XP_016881730.1:n.*91G=
|
|
NM_145045.5:c.1197G=
MANE Select
|
NP_659482.3:p.Leu399=
|
|
NM_001302454.2:c.1017G=
|
NP_001289383.1:p.Leu339=
|
|