ENST00000366425.4:c.621_*1del
(GP1BB)
MANE Select
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ENSP00000383382.2:n.[c.621_*1del;Ter207TrpextTer?]
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ENST00000366425.3:c.621_*1del
(GP1BB)
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ENSP00000383382.2:n.[c.621_*1del;Ter207TrpextTer?]
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ENST00000431044.5:c.*1706_*1707del
(SEPTIN5)
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ENSP00000399685.1:n.*1706_*1707del
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NM_000407.4:c.621_*1del , LRG_478t1:c.621_*1del
(GP1BB)
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NP_000398.1:n.[c.621_*1del;Ter207TrpextTer?]
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NR_037611.1:n.4361_4362del
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NR_037612.1:n.2865_2866del
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NM_000407.5:c.621_*1del
(GP1BB)
MANE Select
|
NP_000398.1:n.[c.621_*1del;Ter207TrpextTer?]
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