ENST00000394867.9:n.1617G>T
|
|
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ENST00000688002.1:n.3329G>T
|
|
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ENST00000688751.1:n.314G>T
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|
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ENST00000689792.1:n.1082G>T
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|
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ENST00000262948.10:c.1178G>T
MANE Select
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ENSP00000262948.4:p.Gly393Val
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ENST00000262948.9:c.1178G>T
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ENSP00000262948.3:p.Gly393Val
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|
ENST00000394867.8:c.887G>T
|
ENSP00000378336.1:p.Gly296Val
|
|
ENST00000597263.5:n.363G>T
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|
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ENST00000599021.1:c.288G>T
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|
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ENST00000600584.5:n.2627G>T
|
|
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ENST00000601786.5:n.1479G>T
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|
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NM_030662.3:c.1178G>T , LRG_750t1:c.1178G>T
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NP_109587.1:p.Gly393Val
|
|
XM_006722799.2:c.899G>T
|
XP_006722862.1:p.Gly300Val
|
|
XM_011528133.1:c.608G>T
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XP_011526435.1:p.Gly203Val
|
|
NM_030662.4:c.1178G>T
MANE Select
|
NP_109587.1:p.Gly393Val
|
|