ENST00000578493.2:n.798_803dup
|
|
|
ENST00000699291.1:c.590_595dup
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ENSP00000514272.1:n.590_595dup
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ENST00000699292.1:n.505_510dup
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|
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ENST00000225275.4:c.1465_1470dup
MANE Select
|
ENSP00000225275.3:p.Ile490_Ala491insArgIle
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ENST00000225275.3:c.1465_1470dup
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ENSP00000225275.3:p.Ile490_Ala491insArgIle
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NM_000250.1:c.1465_1470dup , LRG_84t1:c.1465_1470dup
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NP_000241.1:p.Ile490_Ala491insArgIle
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|
XM_011524821.1:c.1651_1656dup
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XP_011523123.1:p.Ile552_Ala553insArgIle
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XM_011524822.1:c.1180_1185dup
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XP_011523124.1:p.Ile395_Ala396insArgIle
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|
XM_011524823.1:c.*14_*19dup
|
XP_011523125.1:n.*14_*19dup
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|
NM_000250.2:c.1465_1470dup
MANE Select
|
NP_000241.1:p.Ile490_Ala491insArgIle
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