ENST00000493477.2:n.1179G>T
|
|
|
ENST00000682162.1:c.705G>T
|
ENSP00000508203.1:n.705G>T
|
|
ENST00000682567.1:n.753G>T
|
|
|
ENST00000683521.1:c.676G>T
|
ENSP00000506864.1:p.Ala226Ser
|
|
ENST00000684161.1:n.1891G>T
|
|
|
ENST00000684483.1:c.*72G>T
|
ENSP00000507894.1:n.*72G>T
|
|
ENST00000366560.4:c.676G>T
MANE Select
|
ENSP00000355518.4:p.Ala226Ser
|
|
ENST00000366560.3:c.676G>T
|
ENSP00000355518.3:p.Ala226Ser
|
|
NM_000143.3:c.676G>T , LRG_504t1:c.676G>T
|
NP_000134.2:p.Ala226Ser
|
|
XM_011544132.1:c.448G>T
|
XP_011542434.1:p.Ala150Ser
|
|
XM_011544132.2:c.448G>T
|
XP_011542434.1:p.Ala150Ser
|
|
NM_000143.4:c.676G>T
MANE Select
|
NP_000134.2:p.Ala226Ser
|
|