ENST00000339394.7:c.622G=
MANE Select
|
ENSP00000344468.6:p.Val208=
|
|
ENST00000336798.11:c.448G=
|
ENSP00000338346.7:p.Val150=
|
|
ENST00000339394.6:c.622G=
|
ENSP00000344468.6:p.Val208=
|
|
ENST00000471567.1:n.556G=
|
|
|
NM_014654.3:c.622G=
|
NP_055469.3:p.Val208=
|
|
XM_011542462.1:c.625G=
|
XP_011540764.1:p.Val209=
|
|
XM_011542463.1:c.589G=
|
XP_011540765.1:p.Val197=
|
|
XM_011542464.1:c.586G=
|
XP_011540766.1:p.Val196=
|
|
XM_011542465.1:c.547G=
|
XP_011540767.1:p.Val183=
|
|
XM_011542466.1:c.496G=
|
XP_011540768.1:p.Val166=
|
|
XM_011542464.2:c.586G=
|
XP_011540766.1:p.Val196=
|
|
NM_014654.4:c.622G=
MANE Select
|
NP_055469.3:p.Val208=
|
|