ENST00000309755.9:c.1021+218G=
MANE Select
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ENSP00000312397.4:n.1021+218G=
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ENST00000309755.8:c.1021+218G=
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ENSP00000312397.4:n.1021+218G=
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|
ENST00000502381.1:n.608+218G=
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|
|
ENST00000504208.5:c.*335-11205G=
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ENSP00000423585.1:n.*335-11205G=
|
|
ENST00000505853.1:c.901+218G=
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ENSP00000426173.1:n.901+218G=
|
|
ENST00000506491.5:c.775+218G=
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ENSP00000424828.1:n.775+218G=
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|
ENST00000506873.5:n.646+218G=
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|
|
ENST00000508657.5:c.925+218G=
|
ENSP00000422099.1:n.925+218G=
|
|
NM_001257194.1:c.925+218G=
|
NP_001244123.1:n.925+218G=
|
|
NM_001257195.1:c.775+218G=
|
NP_001244124.1:n.775+218G=
|
|
NM_017415.2:c.1021+218G=
|
NP_059111.2:n.1021+218G=
|
|
NM_017415.3:c.1021+218G=
MANE Select
|
NP_059111.2:n.1021+218G=
|
|
NM_001257195.2:c.775+218G=
|
NP_001244124.1:n.775+218G=
|
|