ENST00000267845.8:c.1804G>T
MANE Select
|
ENSP00000267845.3:p.Ala602Ser
|
|
ENST00000267845.7:c.1804G>T
|
ENSP00000267845.3:p.Ala602Ser
|
|
ENST00000543581.5:c.1705G>T
|
ENSP00000440252.1:p.Ala569Ser
|
|
ENST00000559816.1:n.1548G>T
|
|
|
NM_001306146.1:c.1705G>T
|
NP_001293075.1:p.Ala569Ser
|
|
NM_002112.3:c.1804G>T
|
NP_002103.2:p.Ala602Ser
|
|
XM_011521479.1:c.1567G>T
|
XP_011519781.1:p.Ala523Ser
|
|
XM_011521480.1:c.1372G>T
|
XP_011519782.1:p.Ala458Ser
|
|
XM_017022094.1:c.1909G>T
|
XP_016877583.1:p.Ala637Ser
|
|
XM_017022095.1:c.1810G>T
|
XP_016877584.1:p.Ala604Ser
|
|
XM_017022096.1:c.1681G>T
|
XP_016877585.1:p.Ala561Ser
|
|
XM_017022097.1:c.1672G>T
|
XP_016877586.1:p.Ala558Ser
|
|
XM_017022098.1:c.1477G>T
|
XP_016877587.1:p.Ala493Ser
|
|
NM_002112.4:c.1804G>T
MANE Select
|
NP_002103.2:p.Ala602Ser
|
|
NM_001306146.2:c.1705G>T
|
NP_001293075.1:p.Ala569Ser
|
|