ENST00000394867.9:n.1331C>G
|
|
|
ENST00000687128.1:n.1331C>G
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|
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ENST00000688002.1:n.1186C>G
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|
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ENST00000689792.1:n.796C>G
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|
|
ENST00000262948.10:c.892C>G
MANE Select
|
ENSP00000262948.4:p.Pro298Ala
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ENST00000262948.9:c.892C>G
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ENSP00000262948.3:p.Pro298Ala
|
|
ENST00000394867.8:c.601C>G
|
ENSP00000378336.1:p.Pro201Ala
|
|
ENST00000593364.5:n.839C>G
|
|
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ENST00000595715.1:n.707C>G
|
|
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ENST00000597263.5:n.169+1791C>G
|
|
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ENST00000599021.1:c.29+1791C>G
|
|
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ENST00000600584.5:n.1452C>G
|
|
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ENST00000601786.5:n.1193C>G
|
|
|
NM_030662.3:c.892C>G , LRG_750t1:c.892C>G
|
NP_109587.1:p.Pro298Ala
|
|
XM_006722799.2:c.705+1791C>G
|
XP_006722862.1:n.705+1791C>G
|
|
XM_011528133.1:c.322C>G
|
XP_011526435.1:p.Pro108Ala
|
|
XM_017026989.1:c.892C>G
|
XP_016882478.1:p.Pro298Ala
|
|
XM_017026990.1:c.705+1791C>G
|
XP_016882479.1:n.705+1791C>G
|
|
NM_030662.4:c.892C>G
MANE Select
|
NP_109587.1:p.Pro298Ala
|
|