ENST00000296412.14:c.12+836T>A
MANE Select
|
ENSP00000296412.8:n.12+836T>A
|
|
ENST00000296412.13:c.12+836T>A
|
ENSP00000296412.8:n.12+836T>A
|
|
ENST00000296412.12:c.12+836T>A
|
ENSP00000296412.8:n.12+836T>A
|
|
ENST00000502386.1:c.12+836T>A
|
ENSP00000427026.1:n.12+836T>A
|
|
ENST00000502590.5:c.12+836T>A
|
ENSP00000422119.1:n.12+836T>A
|
|
ENST00000505652.1:c.12+836T>A
|
ENSP00000421556.1:n.12+836T>A
|
|
ENST00000507102.5:n.25+836T>A
|
|
|
ENST00000508146.5:n.113+836T>A
|
|
|
ENST00000508511.5:n.29+836T>A
|
|
|
ENST00000512659.5:c.12+836T>A
|
ENSP00000424650.1:n.12+836T>A
|
|
ENST00000626055.2:c.12+836T>A
|
ENSP00000487496.1:n.12+836T>A
|
|
NM_000671.4:c.12+836T>A
MANE Select
|
NP_000662.3:n.12+836T>A
|
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