ENST00000578493.2:n.735G>T
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|
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ENST00000699291.1:c.527G>T
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ENSP00000514272.1:p.Gly176Val
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ENST00000699292.1:n.442G>T
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ENST00000225275.4:c.1402G>T
MANE Select
|
ENSP00000225275.3:p.Gly468Trp
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ENST00000225275.3:c.1402G>T
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ENSP00000225275.3:p.Gly468Trp
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NM_000250.1:c.1402G>T , LRG_84t1:c.1402G>T
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NP_000241.1:p.Gly468Trp
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XM_011524821.1:c.1588G>T
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XP_011523123.1:p.Gly530Trp
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XM_011524822.1:c.1117G>T
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XP_011523124.1:p.Gly373Trp
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XM_011524823.1:c.1427G>T
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XP_011523125.1:p.Gly476Val
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NM_000250.2:c.1402G>T
MANE Select
|
NP_000241.1:p.Gly468Trp
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