ENST00000336926.11:c.504C>T
MANE Select
|
ENSP00000336747.6:p.Arg168=
|
|
ENST00000336926.10:c.504C>T
|
ENSP00000336747.6:p.Arg168=
|
|
ENST00000420909.1:c.417C>T
|
ENSP00000414280.1:p.Arg139=
|
|
ENST00000434438.6:c.504C>T
|
ENSP00000410300.2:p.Arg168=
|
|
ENST00000616821.4:c.417C>T
|
ENSP00000484528.1:p.Arg139=
|
|
NM_001243198.2:c.504C>T
|
NP_001230127.1:p.Arg168=
|
|
NM_005338.6:c.504C>T
|
NP_005329.3:p.Arg168=
|
|
XM_005250304.2:c.417C>T
|
XP_005250361.1:p.Arg139=
|
|
XM_005250305.2:c.402C>T
|
XP_005250362.1:p.Arg134=
|
|
XM_011516116.1:c.504C>T
|
XP_011514418.1:p.Arg168=
|
|
XM_011516116.2:c.504C>T
|
XP_011514418.1:p.Arg168=
|
|
XM_017012099.1:c.462C>T
|
XP_016867588.1:p.Arg154=
|
|
NM_005338.7:c.504C>T
MANE Select
|
NP_005329.3:p.Arg168=
|
|
NM_001243198.3:c.504C>T
|
NP_001230127.1:p.Arg168=
|
|
NM_001382444.1:c.402C>T
|
NP_001369373.1:p.Arg134=
|
|
NM_001382445.1:c.417C>T
|
NP_001369374.1:p.Arg139=
|
|