ENST00000355832.10:c.2920C>T
MANE Select
|
ENSP00000348089.5:p.His974Tyr
|
|
ENST00000681632.1:n.4323C>T
|
|
|
ENST00000681659.1:c.2761C>T
|
ENSP00000505631.1:p.His921Tyr
|
|
ENST00000355832.9:c.2920C>T
|
ENSP00000348089.5:p.His974Tyr
|
|
ENST00000623073.3:c.*1216C>T
|
ENSP00000485650.1:n.*1216C>T
|
|
ENST00000623115.3:c.1030C>T
|
ENSP00000485321.1:p.His344Tyr
|
|
ENST00000624341.3:c.752C>T
|
|
|
NM_000124.3:c.2920C>T
|
NP_000115.1:p.His974Tyr
|
|
XR_945953.1:n.690-323G>A
|
|
|
NM_001346440.1:c.2920C>T
|
NP_001333369.1:p.His974Tyr
|
|
NM_000124.4:c.2920C>T
MANE Select
|
NP_000115.1:p.His974Tyr
|
|
NM_001346440.2:c.2920C>T
|
NP_001333369.1:p.His974Tyr
|
|