ENST00000502274.2:c.2164G>T
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|
|
ENST00000515425.6:c.2268G>T
MANE Select
|
ENSP00000423660.1:p.Gln756His
|
|
ENST00000675793.1:c.*1552G>T
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ENSP00000502039.1:n.*1552G>T
|
|
ENST00000676056.1:c.*1778G>T
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ENSP00000501827.1:n.*1778G>T
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|
ENST00000323829.9:c.*1656G>T
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ENSP00000313025.5:n.*1656G>T
|
|
ENST00000504517.5:c.1798G>T
|
ENSP00000421779.1:n.1798G>T
|
|
ENST00000504690.5:c.2268G>T
|
ENSP00000425627.1:p.Gln756His
|
|
ENST00000510779.1:c.1318G>T
|
|
|
ENST00000511307.5:c.*2048G>T
|
ENSP00000421420.1:n.*2048G>T
|
|
ENST00000512049.5:c.2247G>T
|
ENSP00000421860.1:p.Gln749His
|
|
ENST00000513604.5:c.*1656G>T
|
ENSP00000423111.1:n.*1656G>T
|
|
ENST00000515425.5:c.2268G>T
|
ENSP00000423660.1:p.Gln756His
|
|
NM_024577.3:c.2268G>T , LRG_269t1:c.2268G>T
|
NP_078853.2:p.Gln756His
|
|
NM_024577.4:c.2268G>T
MANE Select
|
NP_078853.2:p.Gln756His
|
|