ENST00000355832.10:c.3395C>A
MANE Select
|
ENSP00000348089.5:p.Ser1132Tyr
|
|
ENST00000679552.1:n.466C>A
|
|
|
ENST00000679871.1:n.541C>A
|
|
|
ENST00000679974.1:n.444C>A
|
|
|
ENST00000681632.1:n.4798C>A
|
|
|
ENST00000681659.1:c.3236C>A
|
ENSP00000505631.1:p.Ser1079Tyr
|
|
ENST00000355832.9:c.3395C>A
|
ENSP00000348089.5:p.Ser1132Tyr
|
|
ENST00000623073.3:c.*1691C>A
|
ENSP00000485650.1:n.*1691C>A
|
|
ENST00000623115.3:c.1505C>A
|
ENSP00000485321.1:p.Ser502Tyr
|
|
ENST00000624341.3:c.1227C>A
|
|
|
NM_000124.3:c.3395C>A
|
NP_000115.1:p.Ser1132Tyr
|
|
XR_945953.1:n.243-1000G>T
|
|
|
NM_001346440.1:c.3395C>A
|
NP_001333369.1:p.Ser1132Tyr
|
|
NM_000124.4:c.3395C>A
MANE Select
|
NP_000115.1:p.Ser1132Tyr
|
|
NM_001346440.2:c.3395C>A
|
NP_001333369.1:p.Ser1132Tyr
|
|