ENST00000225964.10:c.3228_3229insGCT
MANE Select
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ENSP00000225964.6:p.Gly1076_Pro1077insAla
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ENST00000225964.9:c.3228_3229insGCT
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ENSP00000225964.5:p.Gly1076_Pro1077insAla
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ENST00000486572.1:n.426_427insGCT
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ENST00000511732.1:n.552_553insGCT
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NM_000088.3:c.3228_3229insGCT , LRG_1t1:c.3228_3229insGCT
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NP_000079.2:p.Gly1076_Pro1077insAla
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XM_005257058.3:c.2958_2959insGCT
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XP_005257115.2:p.Gly986_Pro987insAla
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XM_005257059.3:c.2310_2311insGCT
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XP_005257116.2:p.Gly770_Pro771insAla
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XM_011524341.1:c.3030_3031insGCT
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XP_011522643.1:p.Gly1010_Pro1011insAla
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XM_005257058.4:c.2958_2959insGCT
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XP_005257115.2:p.Gly986_Pro987insAla
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XM_005257059.4:c.2310_2311insGCT
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XP_005257116.2:p.Gly770_Pro771insAla
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NM_000088.4:c.3228_3229insGCT
MANE Select
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NP_000079.2:p.Gly1076_Pro1077insAla
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