ENST00000355832.10:c.2919C>T
MANE Select
|
ENSP00000348089.5:p.Tyr973=
|
|
ENST00000681632.1:n.4322C>T
|
|
|
ENST00000681659.1:c.2760C>T
|
ENSP00000505631.1:p.Tyr920=
|
|
ENST00000355832.9:c.2919C>T
|
ENSP00000348089.5:p.Tyr973=
|
|
ENST00000623073.3:c.*1215C>T
|
ENSP00000485650.1:n.*1215C>T
|
|
ENST00000623115.3:c.1029C>T
|
ENSP00000485321.1:p.Tyr343=
|
|
ENST00000624341.3:c.751C>T
|
|
|
NM_000124.3:c.2919C>T
|
NP_000115.1:p.Tyr973=
|
|
XR_945953.1:n.690-322G>A
|
|
|
NM_001346440.1:c.2919C>T
|
NP_001333369.1:p.Tyr973=
|
|
NM_000124.4:c.2919C>T
MANE Select
|
NP_000115.1:p.Tyr973=
|
|
NM_001346440.2:c.2919C>T
|
NP_001333369.1:p.Tyr973=
|
|