|
ENST00000367698.4:c.1005G=
MANE Select
|
ENSP00000356671.3:p.Val335=
|
|
|
ENST00000367698.3:c.1005G=
|
ENSP00000356671.3:p.Val335=
|
|
|
ENST00000617423.4:c.559+2164G=
|
ENSP00000478688.1:n.559+2164G=
|
|
|
NM_000488.3:c.1005G= , LRG_577t1:c.1005G=
|
NP_000479.1:p.Val335=
|
|
|
XM_005245198.2:c.861G=
|
XP_005245255.1:p.Val287=
|
|
|
NM_001365052.1:c.861G=
|
NP_001351981.1:p.Val287=
|
|
|
NM_000488.4:c.1005G=
MANE Select
|
NP_000479.1:p.Val335=
|
|
|
NM_001365052.2:c.861G=
|
NP_001351981.1:p.Val287=
|
|
|
NM_001386302.1:c.1128G=
|
NP_001373231.1:p.Val376=
|
|
|
NM_001386303.1:c.1086G=
|
NP_001373232.1:p.Val362=
|
|
|
NM_001386304.1:c.984G=
|
NP_001373233.1:p.Val328=
|
|
|
NM_001386305.1:c.948G=
|
NP_001373234.1:p.Val316=
|
|
|
NM_001386306.1:c.789G=
|
NP_001373235.1:p.Val263=
|
|
