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NM_006947.4:c.19G>T
MANE Select
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NP_008878.3:p.Gly7Trp
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ENST00000642900.1:c.19G>T
MANE Select
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ENSP00000495128.1:p.Gly7Trp
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NM_001267722.1:c.19G>T
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NP_001254651.1:p.Gly7Trp
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NM_001267722.2:c.19G>T
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NP_001254651.1:p.Gly7Trp
|
|
NM_006947.3:c.19G>T
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NP_008878.3:p.Gly7Trp
|
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NR_151856.1:n.59G>T
|
|
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NR_151856.2:n.38G>T
|
|
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ENST00000342756.9:c.19G>T
|
ENSP00000342181.5:p.Gly7Trp
|
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ENST00000504757.2:c.19G>T
|
ENSP00000473576.1:p.Gly7Trp
|
|
ENST00000510663.5:c.19G>T
|
ENSP00000424576.1:p.Gly7Trp
|
|
ENST00000510663.6:c.19G>T
|
ENSP00000424576.1:p.Gly7Trp
|
|
XM_005265765.3:c.19G>T
|
XP_005265822.2:p.Gly7Trp
|
|
XM_024454192.1:c.19G>T
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XP_024309960.1:p.Gly7Trp
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