|
NM_001018111.3:c.1101+122C=
MANE Select
|
NP_001018121.1:n.1101+122C=
|
|
ENST00000378555.8:c.1101+122C=
MANE Select
|
ENSP00000367817.3:n.1101+122C=
|
|
NM_001018111.2:c.1101+122C=
|
NP_001018121.1:n.1101+122C=
|
|
NM_005397.3:c.1005+122C=
|
NP_005388.2:n.1005+122C=
|
|
NM_005397.4:c.1005+122C=
|
NP_005388.2:n.1005+122C=
|
|
ENST00000322985.9:c.1005+122C=
|
ENSP00000319782.9:n.1005+122C=
|
|
ENST00000378555.7:c.1101+122C=
|
ENSP00000367817.3:n.1101+122C=
|
|
ENST00000446198.5:c.*366+122C=
|
ENSP00000390152.1:n.*366+122C=
|
|
ENST00000487965.1:n.452+122C=
|
|