ENST00000314251.8:c.1366T>C
MANE Select
|
ENSP00000323568.3:p.Tyr456His
|
|
ENST00000314251.7:c.1366T>C
|
ENSP00000323568.3:p.Tyr456His
|
|
ENST00000469787.1:c.*833T>C
|
ENSP00000417918.1:n.*833T>C
|
|
ENST00000497642.5:c.*833T>C
|
ENSP00000418456.1:n.*833T>C
|
|
NM_000340.1:c.1366T>C
|
NP_000331.1:p.Tyr456His
|
|
NM_001278658.1:c.1009T>C
|
NP_001265587.1:p.Tyr337His
|
|
NM_001278659.1:c.847T>C
|
NP_001265588.1:p.Tyr283His
|
|
XM_011513087.1:c.1321T>C
|
XP_011511389.1:p.Tyr441His
|
|
XM_011513088.1:c.1147T>C
|
XP_011511390.1:p.Tyr383His
|
|
XM_011513089.1:c.847T>C
|
XP_011511391.1:p.Tyr283His
|
|
XM_011513087.2:c.1321T>C
|
XP_011511389.1:p.Tyr441His
|
|
XM_024453720.1:c.847T>C
|
XP_024309488.1:p.Tyr283His
|
|
NM_000340.2:c.1366T>C
MANE Select
|
NP_000331.1:p.Tyr456His
|
|
NM_001278658.2:c.1009T>C
|
NP_001265587.1:p.Tyr337His
|
|
NM_001278659.2:c.847T>C
|
NP_001265588.1:p.Tyr283His
|
|