ENST00000267845.8:c.1778G>T
MANE Select
|
ENSP00000267845.3:p.Ser593Ile
|
|
ENST00000267845.7:c.1778G>T
|
ENSP00000267845.3:p.Ser593Ile
|
|
ENST00000543581.5:c.1679G>T
|
ENSP00000440252.1:p.Ser560Ile
|
|
ENST00000559816.1:n.1522G>T
|
|
|
NM_001306146.1:c.1679G>T
|
NP_001293075.1:p.Ser560Ile
|
|
NM_002112.3:c.1778G>T
|
NP_002103.2:p.Ser593Ile
|
|
XM_011521479.1:c.1541G>T
|
XP_011519781.1:p.Ser514Ile
|
|
XM_011521480.1:c.1346G>T
|
XP_011519782.1:p.Ser449Ile
|
|
XM_017022094.1:c.1883G>T
|
XP_016877583.1:p.Ser628Ile
|
|
XM_017022095.1:c.1784G>T
|
XP_016877584.1:p.Ser595Ile
|
|
XM_017022096.1:c.1655G>T
|
XP_016877585.1:p.Ser552Ile
|
|
XM_017022097.1:c.1646G>T
|
XP_016877586.1:p.Ser549Ile
|
|
XM_017022098.1:c.1451G>T
|
XP_016877587.1:p.Ser484Ile
|
|
NM_002112.4:c.1778G>T
MANE Select
|
NP_002103.2:p.Ser593Ile
|
|
NM_001306146.2:c.1679G>T
|
NP_001293075.1:p.Ser560Ile
|
|