ENST00000267845.8:c.1807T>G
MANE Select
|
ENSP00000267845.3:p.Ser603Ala
|
|
ENST00000267845.7:c.1807T>G
|
ENSP00000267845.3:p.Ser603Ala
|
|
ENST00000543581.5:c.1708T>G
|
ENSP00000440252.1:p.Ser570Ala
|
|
ENST00000559816.1:n.1551T>G
|
|
|
NM_001306146.1:c.1708T>G
|
NP_001293075.1:p.Ser570Ala
|
|
NM_002112.3:c.1807T>G
|
NP_002103.2:p.Ser603Ala
|
|
XM_011521479.1:c.1570T>G
|
XP_011519781.1:p.Ser524Ala
|
|
XM_011521480.1:c.1375T>G
|
XP_011519782.1:p.Ser459Ala
|
|
XM_017022094.1:c.1912T>G
|
XP_016877583.1:p.Ser638Ala
|
|
XM_017022095.1:c.1813T>G
|
XP_016877584.1:p.Ser605Ala
|
|
XM_017022096.1:c.1684T>G
|
XP_016877585.1:p.Ser562Ala
|
|
XM_017022097.1:c.1675T>G
|
XP_016877586.1:p.Ser559Ala
|
|
XM_017022098.1:c.1480T>G
|
XP_016877587.1:p.Ser494Ala
|
|
NM_002112.4:c.1807T>G
MANE Select
|
NP_002103.2:p.Ser603Ala
|
|
NM_001306146.2:c.1708T>G
|
NP_001293075.1:p.Ser570Ala
|
|