|
ENST00000367698.4:c.1245T>C
MANE Select
|
ENSP00000356671.3:p.Ala415=
|
|
|
ENST00000367698.3:c.1245T>C
|
ENSP00000356671.3:p.Ala415=
|
|
|
ENST00000617423.4:c.630T>C
|
ENSP00000478688.1:p.Ala210=
|
|
|
NM_000488.3:c.1245T>C , LRG_577t1:c.1245T>C
|
NP_000479.1:p.Ala415=
|
|
|
XM_005245198.2:c.1101T>C
|
XP_005245255.1:p.Ala367=
|
|
|
NM_001365052.1:c.1101T>C
|
NP_001351981.1:p.Ala367=
|
|
|
NM_000488.4:c.1245T>C
MANE Select
|
NP_000479.1:p.Ala415=
|
|
|
NM_001365052.2:c.1101T>C
|
NP_001351981.1:p.Ala367=
|
|
|
NM_001386302.1:c.1368T>C
|
NP_001373231.1:p.Ala456=
|
|
|
NM_001386303.1:c.1326T>C
|
NP_001373232.1:p.Ala442=
|
|
|
NM_001386304.1:c.1224T>C
|
NP_001373233.1:p.Ala408=
|
|
|
NM_001386305.1:c.1188T>C
|
NP_001373234.1:p.Ala396=
|
|
|
NM_001386306.1:c.1029T>C
|
NP_001373235.1:p.Ala343=
|
|
