ENST00000392676.8:c.4346G>T
MANE Select
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ENSP00000376443.2:p.Gly1449Val
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ENST00000392676.7:c.4346G>T
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ENSP00000376443.2:p.Gly1449Val
|
|
ENST00000586811.1:c.1244G>T
|
ENSP00000465351.1:p.Gly415Val
|
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ENST00000586995.5:c.3408G>T
|
ENSP00000467251.1:n.3408G>T
|
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ENST00000588877.5:c.4346G>T
|
ENSP00000467882.1:p.Gly1449Val
|
|
ENST00000591234.5:c.2288G>T
|
ENSP00000465766.1:n.2288G>T
|
|
NM_018672.4:c.4346G>T
|
NP_061142.2:p.Gly1449Val
|
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NM_172232.3:c.4346G>T
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NP_758424.1:p.Gly1449Val
|
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NM_172232.4:c.4346G>T
MANE Select
|
NP_758424.1:p.Gly1449Val
|
|
NM_018672.5:c.4346G>T
|
NP_061142.2:p.Gly1449Val
|
|