ENST00000502274.2:c.2923G>C
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|
|
ENST00000515425.6:c.3027G>C
MANE Select
|
ENSP00000423660.1:p.Gln1009His
|
|
ENST00000675793.1:c.*2311G>C
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ENSP00000502039.1:n.*2311G>C
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|
ENST00000676056.1:c.*2537G>C
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ENSP00000501827.1:n.*2537G>C
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ENST00000323829.9:c.*2415G>C
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ENSP00000313025.5:n.*2415G>C
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|
ENST00000504517.5:c.2557G>C
|
ENSP00000421779.1:n.2557G>C
|
|
ENST00000504690.5:c.3027G>C
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ENSP00000425627.1:p.Gln1009His
|
|
ENST00000510779.1:c.2077G>C
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|
|
ENST00000511307.5:c.*2914G>C
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ENSP00000421420.1:n.*2914G>C
|
|
ENST00000512049.5:c.3006G>C
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ENSP00000421860.1:p.Gln1002His
|
|
ENST00000513604.5:c.*2522G>C
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ENSP00000423111.1:n.*2522G>C
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|
ENST00000515425.5:c.3027G>C
|
ENSP00000423660.1:p.Gln1009His
|
|
NM_024577.3:c.3027G>C , LRG_269t1:c.3027G>C
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NP_078853.2:p.Gln1009His
|
|
NM_024577.4:c.3027G>C
MANE Select
|
NP_078853.2:p.Gln1009His
|
|