ENST00000355832.10:c.3145G>T
MANE Select
|
ENSP00000348089.5:p.Asp1049Tyr
|
|
ENST00000679552.1:n.216G>T
|
|
|
ENST00000679871.1:n.291G>T
|
|
|
ENST00000679974.1:n.194G>T
|
|
|
ENST00000681632.1:n.4548G>T
|
|
|
ENST00000681659.1:c.2986G>T
|
ENSP00000505631.1:p.Asp996Tyr
|
|
ENST00000355832.9:c.3145G>T
|
ENSP00000348089.5:p.Asp1049Tyr
|
|
ENST00000623073.3:c.*1441G>T
|
ENSP00000485650.1:n.*1441G>T
|
|
ENST00000623115.3:c.1255G>T
|
ENSP00000485321.1:p.Asp419Tyr
|
|
ENST00000624341.3:c.977G>T
|
|
|
NM_000124.3:c.3145G>T
|
NP_000115.1:p.Asp1049Tyr
|
|
XR_945953.1:n.243-750C>A
|
|
|
NM_001346440.1:c.3145G>T
|
NP_001333369.1:p.Asp1049Tyr
|
|
NM_000124.4:c.3145G>T
MANE Select
|
NP_000115.1:p.Asp1049Tyr
|
|
NM_001346440.2:c.3145G>T
|
NP_001333369.1:p.Asp1049Tyr
|
|