ENST00000302068.9:c.1146C>G
MANE Select
|
ENSP00000306099.4:p.Ala382=
|
|
ENST00000302068.8:c.1146C>G
|
ENSP00000306099.4:p.Ala382=
|
|
ENST00000502545.5:n.939+394C>G
|
|
|
ENST00000509493.1:c.489C>G
|
ENSP00000426757.1:p.Ala163=
|
|
NM_001184741.1:c.969C>G
|
NP_001171670.1:p.Ala323=
|
|
NM_005141.4:c.1146C>G , LRG_558t1:c.1146C>G
|
NP_005132.2:p.Ala382=
|
|
NM_001382759.1:c.1014C>G
|
NP_001369688.1:p.Ala338=
|
|
NM_001382760.1:c.1146C>G
|
NP_001369689.1:p.Ala382=
|
|
NM_001382761.1:c.1146C>G
|
NP_001369690.1:p.Ala382=
|
|
NM_001382762.1:c.846C>G
|
NP_001369691.1:p.Ala282=
|
|
NM_001382763.1:c.1137C>G
|
NP_001369692.1:p.Ala379=
|
|
NM_001382764.1:c.1080+66C>G
|
NP_001369693.1:n.1080+66C>G
|
|
NM_001382765.1:c.1146C>G
|
NP_001369694.1:p.Ala382=
|
|
NM_005141.5:c.1146C>G
MANE Select
|
NP_005132.2:p.Ala382=
|
|