ENST00000452035.7:n.2029G=
|
|
|
ENST00000483004.2:c.1421G=
|
ENSP00000419887.2:p.Arg474=
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|
ENST00000698628.1:c.1624+228G=
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ENSP00000513848.1:n.1624+228G=
|
|
ENST00000698629.1:n.1814G=
|
|
|
ENST00000698630.1:n.2353G=
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|
|
ENST00000698631.1:n.2354G=
|
|
|
ENST00000698632.1:n.3148G=
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|
|
ENST00000698633.1:n.3038G=
|
|
|
ENST00000698636.1:n.1859G=
|
|
|
ENST00000425368.7:c.1637G=
MANE Select
|
ENSP00000416561.2:p.Arg546=
|
|
ENST00000425368.6:c.1637G=
|
ENSP00000416561.2:p.Arg546=
|
|
ENST00000452035.6:n.1852G=
|
|
|
ENST00000456570.5:c.3143G=
|
ENSP00000410815.1:p.Arg1048=
|
|
ENST00000467360.1:n.763G=
|
|
|
ENST00000477310.1:c.2690G=
|
ENSP00000418996.1:p.Arg897=
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|
ENST00000483004.1:c.259G=
|
|
|
NM_001710.5:c.1637G= , LRG_136t1:c.1637G=
|
NP_001701.2:p.Arg546=
|
|
NM_001710.6:c.1637G=
MANE Select
|
NP_001701.2:p.Arg546=
|
|