ENST00000302068.9:c.1020T>A
MANE Select
|
ENSP00000306099.4:p.Leu340=
|
|
ENST00000302068.8:c.1020T>A
|
ENSP00000306099.4:p.Leu340=
|
|
ENST00000502545.5:n.939+268T>A
|
|
|
ENST00000509493.1:c.363T>A
|
ENSP00000426757.1:p.Leu121=
|
|
NM_001184741.1:c.843T>A
|
NP_001171670.1:p.Leu281=
|
|
NM_005141.4:c.1020T>A , LRG_558t1:c.1020T>A
|
NP_005132.2:p.Leu340=
|
|
NM_001382759.1:c.888T>A
|
NP_001369688.1:p.Leu296=
|
|
NM_001382760.1:c.1020T>A
|
NP_001369689.1:p.Leu340=
|
|
NM_001382761.1:c.1020T>A
|
NP_001369690.1:p.Leu340=
|
|
NM_001382762.1:c.746-26T>A
|
NP_001369691.1:n.746-26T>A
|
|
NM_001382763.1:c.1011T>A
|
NP_001369692.1:p.Leu337=
|
|
NM_001382764.1:c.1020T>A
|
NP_001369693.1:p.Leu340=
|
|
NM_001382765.1:c.1020T>A
|
NP_001369694.1:p.Leu340=
|
|
NM_005141.5:c.1020T>A
MANE Select
|
NP_005132.2:p.Leu340=
|
|