ENST00000255078.8:c.2568A>G
MANE Select
|
ENSP00000255078.4:p.Ser856=
|
|
ENST00000674675.1:c.713A>G
|
|
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ENST00000674878.1:c.673A>G
|
|
|
ENST00000675118.1:c.2056A>G
|
|
|
ENST00000675389.1:n.843A>G
|
|
|
ENST00000675615.1:c.2568A>G
|
ENSP00000502413.1:p.Ser856=
|
|
ENST00000675648.1:n.1943A>G
|
|
|
ENST00000675916.1:c.812A>G
|
|
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ENST00000676173.1:n.3313A>G
|
|
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ENST00000676182.1:c.999A>G
|
|
|
ENST00000676228.1:c.*1891A>G
|
ENSP00000502375.1:n.*1891A>G
|
|
ENST00000255078.7:c.2568A>G
|
ENSP00000255078.3:p.Ser856=
|
|
ENST00000539064.5:n.2327A>G
|
|
|
ENST00000543739.5:n.1561A>G
|
|
|
NM_002180.2:c.2568A>G , LRG_250t1:c.2568A>G
|
NP_002171.2:p.Ser856=
|
|
XM_005273974.2:c.1557A>G
|
XP_005274031.1:p.Ser519=
|
|
XM_005273975.2:c.1440A>G
|
XP_005274032.1:p.Ser480=
|
|
XM_011544994.1:c.1335A>G
|
XP_011543296.1:p.Ser445=
|
|
XR_949903.1:n.2670A>G
|
|
|
XM_005273975.3:c.1440A>G
|
XP_005274032.1:p.Ser480=
|
|
XM_017017669.2:c.1557A>G
|
XP_016873158.1:p.Ser519=
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|
XM_017017670.2:c.1557A>G
|
XP_016873159.1:p.Ser519=
|
|
XR_949903.3:n.2666A>G
|
|
|
NM_002180.3:c.2568A>G
MANE Select
|
NP_002171.2:p.Ser856=
|
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