ENST00000452035.7:n.2335G>C
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|
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ENST00000483004.2:c.1632G>C
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ENSP00000419887.2:p.Gln544His
|
|
ENST00000698628.1:c.1625-207G>C
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ENSP00000513848.1:n.1625-207G>C
|
|
ENST00000698629.1:n.2120G>C
|
|
|
ENST00000698630.1:n.2564G>C
|
|
|
ENST00000698631.1:n.2565G>C
|
|
|
ENST00000698632.1:n.3454G>C
|
|
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ENST00000698633.1:n.3344G>C
|
|
|
ENST00000425368.7:c.1848G>C
MANE Select
|
ENSP00000416561.2:p.Gln616His
|
|
ENST00000425368.6:c.1848G>C
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ENSP00000416561.2:p.Gln616His
|
|
ENST00000456570.5:c.3354G>C
|
ENSP00000410815.1:p.Gln1118His
|
|
ENST00000467360.1:n.974G>C
|
|
|
ENST00000477310.1:c.2901G>C
|
ENSP00000418996.1:p.Gln967His
|
|
ENST00000482312.1:n.64G>C
|
|
|
ENST00000483004.1:c.470G>C
|
|
|
NM_001710.5:c.1848G>C , LRG_136t1:c.1848G>C
|
NP_001701.2:p.Gln616His
|
|
NM_001710.6:c.1848G>C
MANE Select
|
NP_001701.2:p.Gln616His
|
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