ENST00000256906.5:c.406A>G
MANE Select
|
ENSP00000256906.4:p.Met136Val
|
|
ENST00000256906.4:c.406A>G
|
ENSP00000256906.4:p.Met136Val
|
|
ENST00000426880.2:c.194-52A>G
|
ENSP00000402526.2:n.194-52A>G
|
|
NM_001143828.1:c.194-52A>G
|
NP_001137300.1:n.194-52A>G
|
|
NM_001160166.1:c.*38A>G
|
NP_001153638.1:n.*38A>G
|
|
NM_021624.3:c.406A>G
|
NP_067637.2:p.Met136Val
|
|
XM_011526133.1:c.357+7844A>G
|
XP_011524435.1:n.357+7844A>G
|
|
NM_021624.4:c.406A>G
MANE Select
|
NP_067637.2:p.Met136Val
|
|
NM_001143828.2:c.194-52A>G
|
NP_001137300.1:n.194-52A>G
|
|
NM_001160166.2:c.*38A>G
|
NP_001153638.1:n.*38A>G
|
|