ENST00000315491.12:c.1266C>G
MANE Select
|
ENSP00000320295.7:p.Tyr422Ter
|
|
ENST00000680788.1:n.4687C>G
|
|
|
ENST00000315491.11:c.1266C>G
|
ENSP00000320295.7:p.Tyr422Ter
|
|
ENST00000554444.5:c.1050C>G
|
ENSP00000451617.1:p.Tyr350Ter
|
|
ENST00000555576.5:c.277+2139C>G
|
ENSP00000452554.1:n.277+2139C>G
|
|
ENST00000555609.5:c.*1351C>G
|
ENSP00000451276.1:n.*1351C>G
|
|
ENST00000556922.1:c.2307C>G
|
ENSP00000451560.1:p.Tyr769Ter
|
|
NM_001197181.1:c.1050C>G
|
NP_001184110.1:p.Tyr350Ter
|
|
NM_006086.3:c.1266C>G
|
NP_006077.2:p.Tyr422Ter
|
|
NM_006086.4:c.1266C>G
MANE Select
|
NP_006077.2:p.Tyr422Ter
|
|
NM_001197181.2:c.1050C>G
|
NP_001184110.1:p.Tyr350Ter
|
|