ENST00000493477.2:n.929G=
|
|
|
ENST00000682162.1:c.455G=
|
ENSP00000508203.1:n.455G=
|
|
ENST00000682567.1:n.503G=
|
|
|
ENST00000683521.1:c.426G=
|
ENSP00000506864.1:p.Gln142=
|
|
ENST00000684483.1:c.426G=
|
ENSP00000507894.1:p.Gln142=
|
|
ENST00000366560.4:c.426G=
MANE Select
|
ENSP00000355518.4:p.Gln142=
|
|
ENST00000366560.3:c.426G=
|
ENSP00000355518.3:p.Gln142=
|
|
ENST00000497042.1:n.122G=
|
|
|
NM_000143.3:c.426G= , LRG_504t1:c.426G=
|
NP_000134.2:p.Gln142=
|
|
XM_011544132.1:c.198G=
|
XP_011542434.1:p.Gln66=
|
|
XM_011544132.2:c.198G=
|
XP_011542434.1:p.Gln66=
|
|
NM_000143.4:c.426G=
MANE Select
|
NP_000134.2:p.Gln142=
|
|