ENST00000698724.1:n.1815G>T
|
|
|
ENST00000698725.1:n.1568G>T
|
|
|
ENST00000698726.1:n.3128G>T
|
|
|
ENST00000698727.1:n.2861G>T
|
|
|
ENST00000698728.1:n.3477G>T
|
|
|
ENST00000698729.1:n.4925G>T
|
|
|
ENST00000698730.1:n.5023G>T
|
|
|
ENST00000698731.1:c.3757G>T
|
ENSP00000513898.1:p.Val1253Phe
|
|
ENST00000698732.1:c.*2587G>T
|
ENSP00000513899.1:n.*2587G>T
|
|
ENST00000698733.1:c.*3085G>T
|
ENSP00000513900.1:n.*3085G>T
|
|
ENST00000698734.1:c.*2071G>T
|
ENSP00000513901.1:n.*2071G>T
|
|
ENST00000698735.1:n.4249G>T
|
|
|
ENST00000698736.1:n.4662G>T
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|
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ENST00000698737.1:n.4013G>T
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|
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ENST00000372371.8:c.3898G>T
MANE Select
|
ENSP00000361446.3:p.Val1300Phe
|
|
ENST00000372371.7:c.3898G>T
|
ENSP00000361446.3:p.Val1300Phe
|
|
ENST00000616246.4:c.346G>T
|
ENSP00000483738.1:p.Val116Phe
|
|
NM_007055.3:c.3898G>T
|
NP_008986.2:p.Val1300Phe
|
|
NM_007055.4:c.3898G>T
MANE Select
|
NP_008986.2:p.Val1300Phe
|
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