ENST00000698624.1:n.1014C>T
|
|
|
ENST00000006750.8:c.*327C>T
MANE Select
|
ENSP00000006750.4:n.*327C>T
|
|
ENST00000647774.1:c.288+350C>T
|
|
|
ENST00000006750.7:c.*327C>T
|
ENSP00000006750.3:n.*327C>T
|
|
ENST00000392795.7:c.*327C>T
|
ENSP00000376544.3:n.*327C>T
|
|
ENST00000559358.1:n.1028C>T
|
|
|
NM_000626.2:c.*327C>T
|
NP_000617.1:n.*327C>T
|
|
NM_001039933.1:c.*327C>T , LRG_43t1:c.*327C>T
|
NP_001035022.1:n.*327C>T
|
|
NM_021602.2:c.*327C>T
|
NP_067613.1:n.*327C>T
|
|
XM_005257858.3:c.*327C>T
|
XP_005257915.1:n.*327C>T
|
|
NM_000626.3:c.*327C>T
|
NP_000617.1:n.*327C>T
|
|
NM_001039933.2:c.*327C>T
|
NP_001035022.1:n.*327C>T
|
|
NM_001329050.1:c.*327C>T
|
NP_001315979.1:n.*327C>T
|
|
NM_021602.3:c.*327C>T
|
NP_067613.1:n.*327C>T
|
|
NM_000626.4:c.*327C>T
MANE Select
|
NP_000617.1:n.*327C>T
|
|
NM_001039933.3:c.*327C>T
|
NP_001035022.1:n.*327C>T
|
|
NM_001329050.2:c.*327C>T
|
NP_001315979.1:n.*327C>T
|
|
NM_021602.4:c.*327C>T
|
NP_067613.1:n.*327C>T
|
|