ENST00000255078.8:c.1418+2T>A
MANE Select
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ENSP00000255078.4:n.1418+2T>A
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ENST00000674955.1:c.*135+2T>A
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ENSP00000502463.1:n.*135+2T>A
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ENST00000675118.1:c.906+2T>A
|
|
|
ENST00000675205.1:n.183+2T>A
|
|
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ENST00000675615.1:c.1418+2T>A
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ENSP00000502413.1:n.1418+2T>A
|
|
ENST00000675648.1:n.793+2T>A
|
|
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ENST00000675997.1:n.113-981T>A
|
|
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ENST00000676173.1:n.2163+2T>A
|
|
|
ENST00000676228.1:c.*741+2T>A
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ENSP00000502375.1:n.*741+2T>A
|
|
ENST00000255078.7:c.1418+2T>A
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ENSP00000255078.3:n.1418+2T>A
|
|
ENST00000537458.5:n.535+2T>A
|
|
|
ENST00000539064.5:n.1177+2T>A
|
|
|
ENST00000543739.5:n.535+2T>A
|
|
|
NM_002180.2:c.1418+2T>A , LRG_250t1:c.1418+2T>A
|
NP_002171.2:n.1418+2T>A
|
|
XM_005273974.2:c.407+2T>A
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XP_005274031.1:n.407+2T>A
|
|
XM_005273975.2:c.290+2T>A
|
XP_005274032.1:n.290+2T>A
|
|
XM_011544994.1:c.185+2T>A
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XP_011543296.1:n.185+2T>A
|
|
XR_949903.1:n.1520+2T>A
|
|
|
XM_005273975.3:c.290+2T>A
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XP_005274032.1:n.290+2T>A
|
|
XM_017017669.2:c.407+2T>A
|
XP_016873158.1:n.407+2T>A
|
|
XM_017017670.2:c.407+2T>A
|
XP_016873159.1:n.407+2T>A
|
|
XM_017017671.2:c.1418+2T>A
|
XP_016873160.1:n.1418+2T>A
|
|
XR_949903.3:n.1516+2T>A
|
|
|
NM_002180.3:c.1418+2T>A
MANE Select
|
NP_002171.2:n.1418+2T>A
|
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