ENST00000493477.2:n.1015G=
|
|
|
ENST00000682162.1:c.541G=
|
ENSP00000508203.1:n.541G=
|
|
ENST00000682567.1:n.589G=
|
|
|
ENST00000683521.1:c.512G=
|
ENSP00000506864.1:p.Ser171=
|
|
ENST00000684483.1:c.512G=
|
ENSP00000507894.1:p.Ser171=
|
|
ENST00000366560.4:c.512G=
MANE Select
|
ENSP00000355518.4:p.Ser171=
|
|
ENST00000366560.3:c.512G=
|
ENSP00000355518.3:p.Ser171=
|
|
ENST00000497042.1:n.208G=
|
|
|
NM_000143.3:c.512G= , LRG_504t1:c.512G=
|
NP_000134.2:p.Ser171=
|
|
XM_011544132.1:c.284G=
|
XP_011542434.1:p.Ser95=
|
|
XM_011544132.2:c.284G=
|
XP_011542434.1:p.Ser95=
|
|
NM_000143.4:c.512G=
MANE Select
|
NP_000134.2:p.Ser171=
|
|