ENST00000493477.2:n.1217T>G
|
|
|
ENST00000682162.1:c.743T>G
|
ENSP00000508203.1:n.743T>G
|
|
ENST00000682567.1:n.791T>G
|
|
|
ENST00000683521.1:c.714T>G
|
ENSP00000506864.1:p.Asp238Glu
|
|
ENST00000684161.1:n.1929T>G
|
|
|
ENST00000684483.1:c.*110T>G
|
ENSP00000507894.1:n.*110T>G
|
|
ENST00000366560.4:c.714T>G
MANE Select
|
ENSP00000355518.4:p.Asp238Glu
|
|
ENST00000366560.3:c.714T>G
|
ENSP00000355518.3:p.Asp238Glu
|
|
NM_000143.3:c.714T>G , LRG_504t1:c.714T>G
|
NP_000134.2:p.Asp238Glu
|
|
XM_011544132.1:c.486T>G
|
XP_011542434.1:p.Asp162Glu
|
|
XM_011544132.2:c.486T>G
|
XP_011542434.1:p.Asp162Glu
|
|
NM_000143.4:c.714T>G
MANE Select
|
NP_000134.2:p.Asp238Glu
|
|