ENST00000452035.7:n.2308G>A
|
|
|
ENST00000483004.2:c.1605G>A
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ENSP00000419887.2:p.Leu535=
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|
ENST00000698628.1:c.1625-234G>A
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ENSP00000513848.1:n.1625-234G>A
|
|
ENST00000698629.1:n.2093G>A
|
|
|
ENST00000698630.1:n.2537G>A
|
|
|
ENST00000698631.1:n.2538G>A
|
|
|
ENST00000698632.1:n.3427G>A
|
|
|
ENST00000698633.1:n.3317G>A
|
|
|
ENST00000425368.7:c.1821G>A
MANE Select
|
ENSP00000416561.2:p.Leu607=
|
|
ENST00000425368.6:c.1821G>A
|
ENSP00000416561.2:p.Leu607=
|
|
ENST00000456570.5:c.3327G>A
|
ENSP00000410815.1:p.Leu1109=
|
|
ENST00000467360.1:n.947G>A
|
|
|
ENST00000477310.1:c.2874G>A
|
ENSP00000418996.1:p.Leu958=
|
|
ENST00000482312.1:n.37G>A
|
|
|
ENST00000483004.1:c.443G>A
|
|
|
NM_001710.5:c.1821G>A , LRG_136t1:c.1821G>A
|
NP_001701.2:p.Leu607=
|
|
NM_001710.6:c.1821G>A
MANE Select
|
NP_001701.2:p.Leu607=
|
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