ENST00000267845.8:c.1712G>T
MANE Select
|
ENSP00000267845.3:p.Ser571Ile
|
|
ENST00000267845.7:c.1712G>T
|
ENSP00000267845.3:p.Ser571Ile
|
|
ENST00000543581.5:c.1613G>T
|
ENSP00000440252.1:p.Ser538Ile
|
|
ENST00000559816.1:n.1456G>T
|
|
|
NM_001306146.1:c.1613G>T
|
NP_001293075.1:p.Ser538Ile
|
|
NM_002112.3:c.1712G>T
|
NP_002103.2:p.Ser571Ile
|
|
XM_011521479.1:c.1475G>T
|
XP_011519781.1:p.Ser492Ile
|
|
XM_011521480.1:c.1280G>T
|
XP_011519782.1:p.Ser427Ile
|
|
XM_017022094.1:c.1817G>T
|
XP_016877583.1:p.Ser606Ile
|
|
XM_017022095.1:c.1718G>T
|
XP_016877584.1:p.Ser573Ile
|
|
XM_017022096.1:c.1589G>T
|
XP_016877585.1:p.Ser530Ile
|
|
XM_017022097.1:c.1580G>T
|
XP_016877586.1:p.Ser527Ile
|
|
XM_017022098.1:c.1385G>T
|
XP_016877587.1:p.Ser462Ile
|
|
NM_002112.4:c.1712G>T
MANE Select
|
NP_002103.2:p.Ser571Ile
|
|
NM_001306146.2:c.1613G>T
|
NP_001293075.1:p.Ser538Ile
|
|