ENST00000267845.8:c.1846T>G
MANE Select
|
ENSP00000267845.3:p.Ser616Ala
|
|
ENST00000267845.7:c.1846T>G
|
ENSP00000267845.3:p.Ser616Ala
|
|
ENST00000543581.5:c.1747T>G
|
ENSP00000440252.1:p.Ser583Ala
|
|
ENST00000559816.1:n.1590T>G
|
|
|
NM_001306146.1:c.1747T>G
|
NP_001293075.1:p.Ser583Ala
|
|
NM_002112.3:c.1846T>G
|
NP_002103.2:p.Ser616Ala
|
|
XM_011521479.1:c.1609T>G
|
XP_011519781.1:p.Ser537Ala
|
|
XM_011521480.1:c.1414T>G
|
XP_011519782.1:p.Ser472Ala
|
|
XM_017022094.1:c.1951T>G
|
XP_016877583.1:p.Ser651Ala
|
|
XM_017022095.1:c.1852T>G
|
XP_016877584.1:p.Ser618Ala
|
|
XM_017022096.1:c.1723T>G
|
XP_016877585.1:p.Ser575Ala
|
|
XM_017022097.1:c.1714T>G
|
XP_016877586.1:p.Ser572Ala
|
|
XM_017022098.1:c.1519T>G
|
XP_016877587.1:p.Ser507Ala
|
|
NM_002112.4:c.1846T>G
MANE Select
|
NP_002103.2:p.Ser616Ala
|
|
NM_001306146.2:c.1747T>G
|
NP_001293075.1:p.Ser583Ala
|
|