ENST00000493477.2:n.1220T>C
|
|
|
ENST00000682162.1:c.746T>C
|
ENSP00000508203.1:n.746T>C
|
|
ENST00000682567.1:n.794T>C
|
|
|
ENST00000683521.1:c.717T>C
|
ENSP00000506864.1:p.Ala239=
|
|
ENST00000684161.1:n.1932T>C
|
|
|
ENST00000684483.1:c.*113T>C
|
ENSP00000507894.1:n.*113T>C
|
|
ENST00000366560.4:c.717T>C
MANE Select
|
ENSP00000355518.4:p.Ala239=
|
|
ENST00000366560.3:c.717T>C
|
ENSP00000355518.3:p.Ala239=
|
|
NM_000143.3:c.717T>C , LRG_504t1:c.717T>C
|
NP_000134.2:p.Ala239=
|
|
XM_011544132.1:c.489T>C
|
XP_011542434.1:p.Ala163=
|
|
XM_011544132.2:c.489T>C
|
XP_011542434.1:p.Ala163=
|
|
NM_000143.4:c.717T>C
MANE Select
|
NP_000134.2:p.Ala239=
|
|