ENST00000355832.10:c.3027T>A
MANE Select
|
ENSP00000348089.5:p.Ser1009Arg
|
|
ENST00000679552.1:n.142-129T>A
|
|
|
ENST00000679871.1:n.173T>A
|
|
|
ENST00000679974.1:n.120-129T>A
|
|
|
ENST00000681632.1:n.4430T>A
|
|
|
ENST00000681659.1:c.2868T>A
|
ENSP00000505631.1:p.Ser956Arg
|
|
ENST00000355832.9:c.3027T>A
|
ENSP00000348089.5:p.Ser1009Arg
|
|
ENST00000623073.3:c.*1323T>A
|
ENSP00000485650.1:n.*1323T>A
|
|
ENST00000623115.3:c.1137T>A
|
ENSP00000485321.1:p.Ser379Arg
|
|
ENST00000624341.3:c.859T>A
|
|
|
NM_000124.3:c.3027T>A
|
NP_000115.1:p.Ser1009Arg
|
|
XR_945953.1:n.243-547A>T
|
|
|
NM_001346440.1:c.3027T>A
|
NP_001333369.1:p.Ser1009Arg
|
|
NM_000124.4:c.3027T>A
MANE Select
|
NP_000115.1:p.Ser1009Arg
|
|
NM_001346440.2:c.3027T>A
|
NP_001333369.1:p.Ser1009Arg
|
|