ENST00000255078.8:c.2119C>G
MANE Select
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ENSP00000255078.4:p.Pro707Ala
|
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ENST00000674675.1:c.363C>G
|
|
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ENST00000674878.1:c.363C>G
|
|
|
ENST00000674955.1:c.*836C>G
|
ENSP00000502463.1:n.*836C>G
|
|
ENST00000675118.1:c.1607C>G
|
|
|
ENST00000675389.1:n.394C>G
|
|
|
ENST00000675615.1:c.2119C>G
|
ENSP00000502413.1:p.Pro707Ala
|
|
ENST00000675648.1:n.1494C>G
|
|
|
ENST00000675916.1:c.363C>G
|
|
|
ENST00000676173.1:n.2864C>G
|
|
|
ENST00000676182.1:c.550C>G
|
|
|
ENST00000676228.1:c.*1442C>G
|
ENSP00000502375.1:n.*1442C>G
|
|
ENST00000255078.7:c.2119C>G
|
ENSP00000255078.3:p.Pro707Ala
|
|
ENST00000539064.5:n.1878C>G
|
|
|
ENST00000543739.5:n.1112C>G
|
|
|
NM_002180.2:c.2119C>G , LRG_250t1:c.2119C>G
|
NP_002171.2:p.Pro707Ala
|
|
XM_005273974.2:c.1108C>G
|
XP_005274031.1:p.Pro370Ala
|
|
XM_005273975.2:c.991C>G
|
XP_005274032.1:p.Pro331Ala
|
|
XM_011544994.1:c.886C>G
|
XP_011543296.1:p.Pro296Ala
|
|
XR_949903.1:n.2221C>G
|
|
|
XM_005273975.3:c.991C>G
|
XP_005274032.1:p.Pro331Ala
|
|
XM_017017669.2:c.1108C>G
|
XP_016873158.1:p.Pro370Ala
|
|
XM_017017670.2:c.1108C>G
|
XP_016873159.1:p.Pro370Ala
|
|
XR_949903.3:n.2217C>G
|
|
|
NM_002180.3:c.2119C>G
MANE Select
|
NP_002171.2:p.Pro707Ala
|
|