ENST00000296412.14:c.345-897T>C
MANE Select
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ENSP00000296412.8:n.345-897T>C
|
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ENST00000296412.13:c.345-897T>C
|
ENSP00000296412.8:n.345-897T>C
|
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ENST00000296412.12:c.345-897T>C
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ENSP00000296412.8:n.345-897T>C
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|
ENST00000502590.5:c.*25-897T>C
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ENSP00000422119.1:n.*25-897T>C
|
|
ENST00000503130.5:c.306-897T>C
|
ENSP00000427049.1:n.306-897T>C
|
|
ENST00000505652.1:c.*169-897T>C
|
ENSP00000421556.1:n.*169-897T>C
|
|
ENST00000508511.5:n.362-897T>C
|
|
|
ENST00000512604.1:n.205-897T>C
|
|
|
ENST00000512621.5:n.333-897T>C
|
|
|
ENST00000512659.5:c.*32-897T>C
|
ENSP00000424650.1:n.*32-897T>C
|
|
ENST00000512991.5:n.543-897T>C
|
|
|
ENST00000626055.2:c.*32-897T>C
|
ENSP00000487496.1:n.*32-897T>C
|
|
NM_000671.4:c.345-897T>C
MANE Select
|
NP_000662.3:n.345-897T>C
|
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