ENST00000394867.9:n.1287T>G
|
|
|
ENST00000687128.1:n.1287T>G
|
|
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ENST00000688002.1:n.1142T>G
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|
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ENST00000689792.1:n.752T>G
|
|
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ENST00000262948.10:c.848T>G
MANE Select
|
ENSP00000262948.4:p.Val283Gly
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|
ENST00000262948.9:c.848T>G
|
ENSP00000262948.3:p.Val283Gly
|
|
ENST00000394867.8:c.557T>G
|
ENSP00000378336.1:p.Val186Gly
|
|
ENST00000593364.5:n.795T>G
|
|
|
ENST00000595715.1:n.663T>G
|
|
|
ENST00000597263.5:n.169+1747T>G
|
|
|
ENST00000599021.1:c.29+1747T>G
|
|
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ENST00000600584.5:n.1408T>G
|
|
|
ENST00000601786.5:n.1149T>G
|
|
|
NM_030662.3:c.848T>G , LRG_750t1:c.848T>G
|
NP_109587.1:p.Val283Gly
|
|
XM_006722799.2:c.705+1747T>G
|
XP_006722862.1:n.705+1747T>G
|
|
XM_011528133.1:c.278T>G
|
XP_011526435.1:p.Val93Gly
|
|
XM_017026989.1:c.848T>G
|
XP_016882478.1:p.Val283Gly
|
|
XM_017026990.1:c.705+1747T>G
|
XP_016882479.1:n.705+1747T>G
|
|
NM_030662.4:c.848T>G
MANE Select
|
NP_109587.1:p.Val283Gly
|
|