ENST00000452035.7:n.1798G=
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|
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ENST00000483004.2:c.1409-219G=
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ENSP00000419887.2:n.1409-219G=
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|
ENST00000698628.1:c.1621G=
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ENSP00000513848.1:p.Val541=
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|
ENST00000698629.1:n.1798G=
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|
|
ENST00000698630.1:n.2337G=
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|
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ENST00000698631.1:n.2338G=
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|
|
ENST00000698632.1:n.2917G=
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|
|
ENST00000698633.1:n.2807G=
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|
|
ENST00000698636.1:n.1843G=
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|
|
ENST00000425368.7:c.1621G=
MANE Select
|
ENSP00000416561.2:p.Val541=
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|
ENST00000425368.6:c.1621G=
|
ENSP00000416561.2:p.Val541=
|
|
ENST00000452035.6:n.1621G=
|
|
|
ENST00000456570.5:c.3127G=
|
ENSP00000410815.1:p.Val1043=
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|
ENST00000467360.1:n.532G=
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|
|
ENST00000477310.1:c.2674G=
|
ENSP00000418996.1:p.Val892=
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|
ENST00000483004.1:c.247-219G=
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|
|
NM_001710.5:c.1621G= , LRG_136t1:c.1621G=
|
NP_001701.2:p.Val541=
|
|
NM_001710.6:c.1621G=
MANE Select
|
NP_001701.2:p.Val541=
|
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