ENST00000267163.6:c.2656G>T
MANE Select
|
ENSP00000267163.4:p.Asp886Tyr
|
|
ENST00000643064.1:c.194+95393G>T
|
|
|
ENST00000650461.1:c.2656G>T
|
ENSP00000497193.1:p.Asp886Tyr
|
|
ENST00000267163.4:c.2656G>T
|
ENSP00000267163.4:p.Asp886Tyr
|
|
ENST00000484879.1:n.390G>T
|
|
|
ENST00000531171.5:n.259G>T
|
|
|
NM_000321.2:c.2656G>T , LRG_517t1:c.2656G>T
|
NP_000312.2:p.Asp886Tyr
|
|
XM_011535171.1:c.2395G>T
|
XP_011533473.1:p.Asp799Tyr
|
|
XM_011535171.2:c.2395G>T
|
XP_011533473.1:p.Asp799Tyr
|
|
NM_000321.3:c.2656G>T
MANE Select
|
NP_000312.2:p.Asp886Tyr
|
|