ENST00000301761.7:c.*115G>T
MANE Select
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ENSP00000301761.3:n.*115G>T
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ENST00000301761.6:c.*115G>T
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ENSP00000301761.2:n.*115G>T
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|
ENST00000536670.5:n.396+8073G>T
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|
|
ENST00000538594.5:c.370+8073G>T
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ENSP00000440939.1:n.370+8073G>T
|
|
ENST00000541135.5:c.377+8066G>T
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ENSP00000443130.1:n.377+8066G>T
|
|
ENST00000542074.1:c.*195G>T
|
ENSP00000469670.1:n.*195G>T
|
|
ENST00000542794.5:c.*618G>T
|
ENSP00000439983.1:n.*618G>T
|
|
ENST00000543044.2:c.*115G>T
|
ENSP00000440219.1:n.*115G>T
|
|
ENST00000544025.5:n.465+8073G>T
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|
|
ENST00000544801.5:c.370+8073G>T
|
ENSP00000442581.1:n.370+8073G>T
|
|
ENST00000544880.1:n.374+8073G>T
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|
|
NM_017841.2:c.*115G>T , LRG_519t1:c.*115G>T
|
NP_060311.1:n.*115G>T
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|
NM_017841.4:c.*115G>T
MANE Select
|
NP_060311.1:n.*115G>T
|
|