ENST00000493477.2:n.701G>T
|
|
|
ENST00000682162.1:c.227G>T
|
ENSP00000508203.1:n.227G>T
|
|
ENST00000682567.1:n.275G>T
|
|
|
ENST00000683521.1:c.198G>T
|
ENSP00000506864.1:p.Lys66Asn
|
|
ENST00000684483.1:c.198G>T
|
ENSP00000507894.1:p.Lys66Asn
|
|
ENST00000366560.4:c.198G>T
MANE Select
|
ENSP00000355518.4:p.Lys66Asn
|
|
ENST00000366560.3:c.198G>T
|
ENSP00000355518.3:p.Lys66Asn
|
|
ENST00000493477.1:n.311G>T
|
|
|
NM_000143.3:c.198G>T , LRG_504t1:c.198G>T
|
NP_000134.2:p.Lys66Asn
|
|
XM_011544132.1:c.-31G>T
|
XP_011542434.1:n.-31G>T
|
|
XM_011544132.2:c.-31G>T
|
XP_011542434.1:n.-31G>T
|
|
NM_000143.4:c.198G>T
MANE Select
|
NP_000134.2:p.Lys66Asn
|
|