ENST00000493477.2:n.1195T>C
|
|
|
ENST00000682162.1:c.721T>C
|
ENSP00000508203.1:n.721T>C
|
|
ENST00000682567.1:n.769T>C
|
|
|
ENST00000683521.1:c.692T>C
|
ENSP00000506864.1:p.Ile231Thr
|
|
ENST00000684161.1:n.1907T>C
|
|
|
ENST00000684483.1:c.*88T>C
|
ENSP00000507894.1:n.*88T>C
|
|
ENST00000366560.4:c.692T>C
MANE Select
|
ENSP00000355518.4:p.Ile231Thr
|
|
ENST00000366560.3:c.692T>C
|
ENSP00000355518.3:p.Ile231Thr
|
|
NM_000143.3:c.692T>C , LRG_504t1:c.692T>C
|
NP_000134.2:p.Ile231Thr
|
|
XM_011544132.1:c.464T>C
|
XP_011542434.1:p.Ile155Thr
|
|
XM_011544132.2:c.464T>C
|
XP_011542434.1:p.Ile155Thr
|
|
NM_000143.4:c.692T>C
MANE Select
|
NP_000134.2:p.Ile231Thr
|
|