ENST00000171111.10:c.1492C>T
MANE Select
|
ENSP00000171111.4:p.Arg498Ter
|
|
ENST00000171111.9:c.1492C>T
|
ENSP00000171111.4:p.Arg498Ter
|
|
ENST00000393623.6:c.1492C>T
|
ENSP00000377245.1:p.Arg498Ter
|
|
ENST00000590593.1:c.305-319C>T
|
|
|
ENST00000592478.5:c.311C>T
|
|
|
NM_012289.3:c.1492C>T
|
NP_036421.2:p.Arg498Ter
|
|
NM_203500.1:c.1492C>T
|
NP_987096.1:p.Arg498Ter
|
|
XM_005260173.1:c.1492C>T
|
XP_005260230.1:p.Arg498Ter
|
|
XM_005260174.1:c.1492C>T
|
XP_005260231.1:p.Arg498Ter
|
|
XM_011528452.1:c.1492C>T
|
XP_011526754.1:p.Arg498Ter
|
|
NM_203500.2:c.1492C>T
MANE Select
|
NP_987096.1:p.Arg498Ter
|
|
NM_012289.4:c.1492C>T
|
NP_036421.2:p.Arg498Ter
|
|