ENST00000309755.9:c.1125G>A
MANE Select
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ENSP00000312397.4:p.Thr375=
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ENST00000309755.8:c.1125G>A
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ENSP00000312397.4:p.Thr375=
|
|
ENST00000502381.1:n.712G>A
|
|
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ENST00000504208.5:c.*335-10610G>A
|
ENSP00000423585.1:n.*335-10610G>A
|
|
ENST00000505853.1:c.1005G>A
|
ENSP00000426173.1:p.Thr335=
|
|
ENST00000506491.5:c.879G>A
|
ENSP00000424828.1:p.Thr293=
|
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ENST00000506873.5:n.750G>A
|
|
|
ENST00000508657.5:c.1029G>A
|
ENSP00000422099.1:p.Thr343=
|
|
NM_001257194.1:c.1029G>A
|
NP_001244123.1:p.Thr343=
|
|
NM_001257195.1:c.879G>A
|
NP_001244124.1:p.Thr293=
|
|
NM_017415.2:c.1125G>A
|
NP_059111.2:p.Thr375=
|
|
NM_017415.3:c.1125G>A
MANE Select
|
NP_059111.2:p.Thr375=
|
|
NM_001257195.2:c.879G>A
|
NP_001244124.1:p.Thr293=
|
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