ENST00000452035.7:n.2069C>G
|
|
|
ENST00000483004.2:c.1461C>G
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ENSP00000419887.2:p.Tyr487Ter
|
|
ENST00000698628.1:c.1624+268C>G
|
ENSP00000513848.1:n.1624+268C>G
|
|
ENST00000698629.1:n.1854C>G
|
|
|
ENST00000698630.1:n.2393C>G
|
|
|
ENST00000698631.1:n.2394C>G
|
|
|
ENST00000698632.1:n.3188C>G
|
|
|
ENST00000698633.1:n.3078C>G
|
|
|
ENST00000698636.1:n.1899C>G
|
|
|
ENST00000425368.7:c.1677C>G
MANE Select
|
ENSP00000416561.2:p.Tyr559Ter
|
|
ENST00000425368.6:c.1677C>G
|
ENSP00000416561.2:p.Tyr559Ter
|
|
ENST00000456570.5:c.3183C>G
|
ENSP00000410815.1:p.Tyr1061Ter
|
|
ENST00000467360.1:n.803C>G
|
|
|
ENST00000477310.1:c.2730C>G
|
ENSP00000418996.1:p.Tyr910Ter
|
|
ENST00000483004.1:c.299C>G
|
|
|
NM_001710.5:c.1677C>G , LRG_136t1:c.1677C>G
|
NP_001701.2:p.Tyr559Ter
|
|
NM_001710.6:c.1677C>G
MANE Select
|
NP_001701.2:p.Tyr559Ter
|
|