ENST00000493477.2:n.1870T>G
|
|
|
ENST00000682162.1:c.1396T>G
|
ENSP00000508203.1:n.1396T>G
|
|
ENST00000682567.1:n.4767T>G
|
|
|
ENST00000683521.1:c.1367T>G
|
ENSP00000506864.1:p.Val456Gly
|
|
ENST00000684161.1:n.2582T>G
|
|
|
ENST00000684483.1:c.*763T>G
|
ENSP00000507894.1:n.*763T>G
|
|
ENST00000366560.4:c.1367T>G
MANE Select
|
ENSP00000355518.4:p.Val456Gly
|
|
ENST00000366560.3:c.1367T>G
|
ENSP00000355518.3:p.Val456Gly
|
|
NM_000143.3:c.1367T>G , LRG_504t1:c.1367T>G
|
NP_000134.2:p.Val456Gly
|
|
XM_011544132.1:c.1139T>G
|
XP_011542434.1:p.Val380Gly
|
|
XM_011544132.2:c.1139T>G
|
XP_011542434.1:p.Val380Gly
|
|
NM_000143.4:c.1367T>G
MANE Select
|
NP_000134.2:p.Val456Gly
|
|