ENST00000255078.8:c.1409A>C
MANE Select
|
ENSP00000255078.4:p.His470Pro
|
|
ENST00000536803.2:n.320A>C
|
|
|
ENST00000674955.1:c.*126A>C
|
ENSP00000502463.1:n.*126A>C
|
|
ENST00000675118.1:c.897A>C
|
|
|
ENST00000675205.1:n.174A>C
|
|
|
ENST00000675310.1:n.546A>C
|
|
|
ENST00000675615.1:c.1409A>C
|
ENSP00000502413.1:p.His470Pro
|
|
ENST00000675648.1:n.784A>C
|
|
|
ENST00000675997.1:n.113-992A>C
|
|
|
ENST00000676149.1:n.483A>C
|
|
|
ENST00000676173.1:n.2154A>C
|
|
|
ENST00000676228.1:c.*732A>C
|
ENSP00000502375.1:n.*732A>C
|
|
ENST00000255078.7:c.1409A>C
|
ENSP00000255078.3:p.His470Pro
|
|
ENST00000537458.5:n.526A>C
|
|
|
ENST00000539064.5:n.1168A>C
|
|
|
ENST00000543739.5:n.526A>C
|
|
|
NM_002180.2:c.1409A>C , LRG_250t1:c.1409A>C
|
NP_002171.2:p.His470Pro
|
|
XM_005273974.2:c.398A>C
|
XP_005274031.1:p.His133Pro
|
|
XM_005273975.2:c.281A>C
|
XP_005274032.1:p.His94Pro
|
|
XM_011544994.1:c.176A>C
|
XP_011543296.1:p.His59Pro
|
|
XR_949903.1:n.1511A>C
|
|
|
XM_005273975.3:c.281A>C
|
XP_005274032.1:p.His94Pro
|
|
XM_017017669.2:c.398A>C
|
XP_016873158.1:p.His133Pro
|
|
XM_017017670.2:c.398A>C
|
XP_016873159.1:p.His133Pro
|
|
XM_017017671.2:c.1409A>C
|
XP_016873160.1:p.His470Pro
|
|
XR_949903.3:n.1507A>C
|
|
|
NM_002180.3:c.1409A>C
MANE Select
|
NP_002171.2:p.His470Pro
|
|