|
ENST00000367698.4:c.1261G=
MANE Select
|
ENSP00000356671.3:p.Val421=
|
|
|
ENST00000367698.3:c.1261G=
|
ENSP00000356671.3:p.Val421=
|
|
|
ENST00000617423.4:c.646G=
|
ENSP00000478688.1:p.Val216=
|
|
|
NM_000488.3:c.1261G= , LRG_577t1:c.1261G=
|
NP_000479.1:p.Val421=
|
|
|
XM_005245198.2:c.1117G=
|
XP_005245255.1:p.Val373=
|
|
|
NM_001365052.1:c.1117G=
|
NP_001351981.1:p.Val373=
|
|
|
NM_000488.4:c.1261G=
MANE Select
|
NP_000479.1:p.Val421=
|
|
|
NM_001365052.2:c.1117G=
|
NP_001351981.1:p.Val373=
|
|
|
NM_001386302.1:c.1384G=
|
NP_001373231.1:p.Val462=
|
|
|
NM_001386303.1:c.1342G=
|
NP_001373232.1:p.Val448=
|
|
|
NM_001386304.1:c.1240G=
|
NP_001373233.1:p.Val414=
|
|
|
NM_001386305.1:c.1204G=
|
NP_001373234.1:p.Val402=
|
|
|
NM_001386306.1:c.1045G=
|
NP_001373235.1:p.Val349=
|
|
