ENST00000452035.7:n.2067T=
|
|
|
ENST00000483004.2:c.1459T=
|
ENSP00000419887.2:p.Tyr487=
|
|
ENST00000698628.1:c.1624+266T=
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ENSP00000513848.1:n.1624+266T=
|
|
ENST00000698629.1:n.1852T=
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|
|
ENST00000698630.1:n.2391T=
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|
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ENST00000698631.1:n.2392T=
|
|
|
ENST00000698632.1:n.3186T=
|
|
|
ENST00000698633.1:n.3076T=
|
|
|
ENST00000698636.1:n.1897T=
|
|
|
ENST00000425368.7:c.1675T=
MANE Select
|
ENSP00000416561.2:p.Tyr559=
|
|
ENST00000425368.6:c.1675T=
|
ENSP00000416561.2:p.Tyr559=
|
|
ENST00000456570.5:c.3181T=
|
ENSP00000410815.1:p.Tyr1061=
|
|
ENST00000467360.1:n.801T=
|
|
|
ENST00000477310.1:c.2728T=
|
ENSP00000418996.1:p.Tyr910=
|
|
ENST00000483004.1:c.297T=
|
|
|
NM_001710.5:c.1675T= , LRG_136t1:c.1675T=
|
NP_001701.2:p.Tyr559=
|
|
NM_001710.6:c.1675T=
MANE Select
|
NP_001701.2:p.Tyr559=
|
|