ENST00000376228.10:c.502_503delinsCA
MANE Select
|
ENSP00000365402.5:p.Gln168=
|
|
ENST00000376228.9:c.502_503delinsCA
|
ENSP00000365402.5:p.Gln168=
|
|
ENST00000376237.8:c.*89_*90delinsCA
|
ENSP00000365412.4:n.*89_*90delinsCA
|
|
ENST00000383329.7:c.502_503delinsCA
|
ENSP00000372819.3:p.Gln168=
|
|
ENST00000415537.1:c.500_501delinsCA
|
|
|
ENST00000484378.1:n.771_772delinsCA
|
|
|
ENST00000487245.5:n.861_862delinsCA
|
|
|
ENST00000495835.1:n.691_692delinsCA
|
|
|
NM_002117.5:c.502_503delinsCA
|
NP_002108.4:p.Gln168=
|
|
NM_002117.6:c.502_503delinsCA
MANE Select
|
NP_002108.4:p.Gln168=
|
|