ENST00000452035.7:n.2154T=
|
|
|
ENST00000483004.2:c.1546T=
|
ENSP00000419887.2:p.Tyr516=
|
|
ENST00000698628.1:c.1624+353T=
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ENSP00000513848.1:n.1624+353T=
|
|
ENST00000698629.1:n.1939T=
|
|
|
ENST00000698630.1:n.2478T=
|
|
|
ENST00000698631.1:n.2479T=
|
|
|
ENST00000698632.1:n.3273T=
|
|
|
ENST00000698633.1:n.3163T=
|
|
|
ENST00000698636.1:n.1984T=
|
|
|
ENST00000425368.7:c.1762T=
MANE Select
|
ENSP00000416561.2:p.Tyr588=
|
|
ENST00000425368.6:c.1762T=
|
ENSP00000416561.2:p.Tyr588=
|
|
ENST00000456570.5:c.3268T=
|
ENSP00000410815.1:p.Tyr1090=
|
|
ENST00000467360.1:n.888T=
|
|
|
ENST00000477310.1:c.2815T=
|
ENSP00000418996.1:p.Tyr939=
|
|
ENST00000483004.1:c.384T=
|
|
|
NM_001710.5:c.1762T= , LRG_136t1:c.1762T=
|
NP_001701.2:p.Tyr588=
|
|
NM_001710.6:c.1762T=
MANE Select
|
NP_001701.2:p.Tyr588=
|
|