ENST00000456935.7:c.1281del
MANE Select
|
ENSP00000395473.2:p.Tyr428MetfsTer?
|
|
ENST00000221363.8:c.1278del
|
ENSP00000221363.4:p.Tyr427MetfsTer?
|
|
ENST00000456935.6:c.1281del
|
ENSP00000395473.2:p.Tyr428MetfsTer?
|
|
ENST00000465830.1:n.445del
|
|
|
ENST00000466794.5:n.1180del
|
|
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ENST00000495617.1:n.281-331del
|
|
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NM_000528.3:c.1281del
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NP_000519.2:p.Tyr428MetfsTer?
|
|
NM_001173498.1:c.1278del
|
NP_001166969.1:p.Tyr427MetfsTer?
|
|
XM_005259913.1:c.1284del
|
XP_005259970.1:p.Tyr429MetfsTer?
|
|
XM_011528017.1:c.180del
|
XP_011526319.1:p.Tyr61MetfsTer?
|
|
XM_005259913.2:c.1284del
|
XP_005259970.1:p.Tyr429MetfsTer?
|
|
XM_024451518.1:c.180del
|
XP_024307286.1:p.Tyr61MetfsTer?
|
|
NM_000528.4:c.1281del
MANE Select
|
NP_000519.2:p.Tyr428MetfsTer?
|
|
NM_001173498.2:c.1278del
|
NP_001166969.1:p.Tyr427MetfsTer?
|
|