ENST00000267845.8:c.1766G>T
MANE Select
|
ENSP00000267845.3:p.Ser589Ile
|
|
ENST00000267845.7:c.1766G>T
|
ENSP00000267845.3:p.Ser589Ile
|
|
ENST00000543581.5:c.1667G>T
|
ENSP00000440252.1:p.Ser556Ile
|
|
ENST00000559816.1:n.1510G>T
|
|
|
NM_001306146.1:c.1667G>T
|
NP_001293075.1:p.Ser556Ile
|
|
NM_002112.3:c.1766G>T
|
NP_002103.2:p.Ser589Ile
|
|
XM_011521479.1:c.1529G>T
|
XP_011519781.1:p.Ser510Ile
|
|
XM_011521480.1:c.1334G>T
|
XP_011519782.1:p.Ser445Ile
|
|
XM_017022094.1:c.1871G>T
|
XP_016877583.1:p.Ser624Ile
|
|
XM_017022095.1:c.1772G>T
|
XP_016877584.1:p.Ser591Ile
|
|
XM_017022096.1:c.1643G>T
|
XP_016877585.1:p.Ser548Ile
|
|
XM_017022097.1:c.1634G>T
|
XP_016877586.1:p.Ser545Ile
|
|
XM_017022098.1:c.1439G>T
|
XP_016877587.1:p.Ser480Ile
|
|
NM_002112.4:c.1766G>T
MANE Select
|
NP_002103.2:p.Ser589Ile
|
|
NM_001306146.2:c.1667G>T
|
NP_001293075.1:p.Ser556Ile
|
|