ENST00000452035.7:n.2129G>C
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|
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ENST00000483004.2:c.1521G>C
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ENSP00000419887.2:p.Leu507=
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|
ENST00000698628.1:c.1624+328G>C
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ENSP00000513848.1:n.1624+328G>C
|
|
ENST00000698629.1:n.1914G>C
|
|
|
ENST00000698630.1:n.2453G>C
|
|
|
ENST00000698631.1:n.2454G>C
|
|
|
ENST00000698632.1:n.3248G>C
|
|
|
ENST00000698633.1:n.3138G>C
|
|
|
ENST00000698636.1:n.1959G>C
|
|
|
ENST00000425368.7:c.1737G>C
MANE Select
|
ENSP00000416561.2:p.Leu579=
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|
ENST00000425368.6:c.1737G>C
|
ENSP00000416561.2:p.Leu579=
|
|
ENST00000456570.5:c.3243G>C
|
ENSP00000410815.1:p.Leu1081=
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|
ENST00000467360.1:n.863G>C
|
|
|
ENST00000477310.1:c.2790G>C
|
ENSP00000418996.1:p.Leu930=
|
|
ENST00000483004.1:c.359G>C
|
|
|
NM_001710.5:c.1737G>C , LRG_136t1:c.1737G>C
|
NP_001701.2:p.Leu579=
|
|
NM_001710.6:c.1737G>C
MANE Select
|
NP_001701.2:p.Leu579=
|
|