ENST00000367698.4:c.846T>C
MANE Select
|
ENSP00000356671.3:p.Ser282=
|
|
ENST00000367698.3:c.846T>C
|
ENSP00000356671.3:p.Ser282=
|
|
ENST00000487183.1:n.497T>C
|
|
|
ENST00000617423.4:c.559+2005T>C
|
ENSP00000478688.1:n.559+2005T>C
|
|
NM_000488.3:c.846T>C , LRG_577t1:c.846T>C
|
NP_000479.1:p.Ser282=
|
|
XM_005245198.2:c.702T>C
|
XP_005245255.1:p.Ser234=
|
|
NM_001365052.1:c.702T>C
|
NP_001351981.1:p.Ser234=
|
|
NM_000488.4:c.846T>C
MANE Select
|
NP_000479.1:p.Ser282=
|
|
NM_001365052.2:c.702T>C
|
NP_001351981.1:p.Ser234=
|
|
NM_001386302.1:c.969T>C
|
NP_001373231.1:p.Ser323=
|
|
NM_001386303.1:c.927T>C
|
NP_001373232.1:p.Ser309=
|
|
NM_001386304.1:c.825T>C
|
NP_001373233.1:p.Ser275=
|
|
NM_001386305.1:c.789T>C
|
NP_001373234.1:p.Ser263=
|
|
NM_001386306.1:c.630T>C
|
NP_001373235.1:p.Ser210=
|
|