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NM_001845.6:c.896G>T
MANE Select
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NP_001836.3:p.Gly299Val
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ENST00000375820.10:c.896G>T
MANE Select
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ENSP00000364979.4:p.Gly299Val
|
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NM_001303110.1:c.896G>T
|
NP_001290039.1:p.Gly299Val
|
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NM_001303110.2:c.896G>T
|
NP_001290039.1:p.Gly299Val
|
|
NM_001845.5:c.896G>T
|
NP_001836.3:p.Gly299Val
|
|
ENST00000375820.8:c.896G>T
|
ENSP00000364979.4:p.Gly299Val
|
|
ENST00000543140.5:c.896G>T
|
ENSP00000443348.1:p.Gly299Val
|
|
ENST00000543140.6:c.896G>T
|
ENSP00000443348.1:p.Gly299Val
|
|
ENST00000615732.2:c.704G>T
|
ENSP00000478222.2:p.Gly235Val
|
|
ENST00000647632.1:n.529G>T
|
|
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ENST00000647797.1:c.775G>T
|
|
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ENST00000649738.1:n.1026G>T
|
|
|
XM_011521048.1:c.704G>T
|
XP_011519350.1:p.Gly235Val
|
|
XM_011521048.2:c.704G>T
|
XP_011519350.1:p.Gly235Val
|