ENST00000493477.2:n.1019G>T
|
|
|
ENST00000682162.1:c.545G>T
|
ENSP00000508203.1:n.545G>T
|
|
ENST00000682567.1:n.593G>T
|
|
|
ENST00000683521.1:c.516G>T
|
ENSP00000506864.1:p.Lys172Asn
|
|
ENST00000684483.1:c.516G>T
|
ENSP00000507894.1:p.Lys172Asn
|
|
ENST00000366560.4:c.516G>T
MANE Select
|
ENSP00000355518.4:p.Lys172Asn
|
|
ENST00000366560.3:c.516G>T
|
ENSP00000355518.3:p.Lys172Asn
|
|
ENST00000497042.1:n.212G>T
|
|
|
NM_000143.3:c.516G>T , LRG_504t1:c.516G>T
|
NP_000134.2:p.Lys172Asn
|
|
XM_011544132.1:c.288G>T
|
XP_011542434.1:p.Lys96Asn
|
|
XM_011544132.2:c.288G>T
|
XP_011542434.1:p.Lys96Asn
|
|
NM_000143.4:c.516G>T
MANE Select
|
NP_000134.2:p.Lys172Asn
|
|