ENST00000258439.8:c.444T>C
MANE Select
|
ENSP00000258439.3:p.Tyr148=
|
|
ENST00000258439.7:c.444T>C
|
ENSP00000258439.2:p.Tyr148=
|
|
ENST00000432959.1:c.444T>C
|
ENSP00000416660.1:p.Tyr148=
|
|
ENST00000435268.1:c.192T>C
|
ENSP00000411810.1:p.Tyr64=
|
|
NM_001193304.2:c.444T>C
|
NP_001180233.1:p.Tyr148=
|
|
NM_017849.3:c.444T>C , LRG_528t1:c.444T>C
|
NP_060319.1:p.Tyr148=
|
|
XM_017004450.1:c.-475T>C
|
XP_016859939.1:n.-475T>C
|
|
XM_017004452.1:c.192T>C
|
XP_016859941.1:p.Tyr64=
|
|
NM_001193304.3:c.444T>C
|
NP_001180233.1:p.Tyr148=
|
|
NM_017849.4:c.444T>C
MANE Select
|
NP_060319.1:p.Tyr148=
|
|