ENST00000340855.11:c.1007-83G=
MANE Select
|
ENSP00000339801.6:n.1007-83G=
|
|
ENST00000651111.1:c.374-83G=
|
ENSP00000498395.1:n.374-83G=
|
|
ENST00000340855.10:c.1007-83G=
|
ENSP00000339801.6:n.1007-83G=
|
|
ENST00000370441.8:c.*107G=
|
ENSP00000359470.4:n.*107G=
|
|
ENST00000422081.6:c.374-83G=
|
ENSP00000477056.1:n.374-83G=
|
|
ENST00000441880.1:n.114-83G=
|
|
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ENST00000466323.5:c.*330G=
|
ENSP00000418264.1:n.*330G=
|
|
ENST00000490775.5:n.924G=
|
|
|
NM_000202.6:c.1007-83G=
|
NP_000193.1:n.1007-83G=
|
|
NM_001166550.2:c.737-83G=
|
NP_001160022.1:n.737-83G=
|
|
NM_006123.4:c.*107G=
|
NP_006114.1:n.*107G=
|
|
NR_104128.1:n.1486G=
|
|
|
NM_000202.7:c.1007-83G=
|
NP_000193.1:n.1007-83G=
|
|
NM_001166550.3:c.737-83G=
|
NP_001160022.1:n.737-83G=
|
|
NM_000202.8:c.1007-83G=
MANE Select
|
NP_000193.1:n.1007-83G=
|
|
NM_001166550.4:c.737-83G=
|
NP_001160022.1:n.737-83G=
|
|
NM_006123.5:c.*107G=
|
NP_006114.1:n.*107G=
|
|
NR_104128.2:n.1438G=
|
|
|