ENST00000502274.2:c.1886G>T
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ENST00000515425.6:c.1990G>T
MANE Select
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ENSP00000423660.1:p.Gly664Ter
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|
ENST00000675793.1:c.*1274G>T
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ENSP00000502039.1:n.*1274G>T
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ENST00000676056.1:c.*1500G>T
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ENSP00000501827.1:n.*1500G>T
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ENST00000323829.9:c.*1378G>T
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ENSP00000313025.5:n.*1378G>T
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ENST00000504517.5:c.1520G>T
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ENSP00000421779.1:n.1520G>T
|
|
ENST00000504690.5:c.1990G>T
|
ENSP00000425627.1:p.Gly664Ter
|
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ENST00000510779.1:c.1040G>T
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|
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ENST00000511307.5:c.*1770G>T
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ENSP00000421420.1:n.*1770G>T
|
|
ENST00000512049.5:c.1969G>T
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ENSP00000421860.1:p.Gly657Ter
|
|
ENST00000513604.5:c.*1378G>T
|
ENSP00000423111.1:n.*1378G>T
|
|
ENST00000515425.5:c.1990G>T
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ENSP00000423660.1:p.Gly664Ter
|
|
NM_024577.3:c.1990G>T , LRG_269t1:c.1990G>T
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NP_078853.2:p.Gly664Ter
|
|
NM_024577.4:c.1990G>T
MANE Select
|
NP_078853.2:p.Gly664Ter
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