ENST00000267845.8:c.1756A>T
MANE Select
|
ENSP00000267845.3:p.Ser586Cys
|
|
ENST00000267845.7:c.1756A>T
|
ENSP00000267845.3:p.Ser586Cys
|
|
ENST00000543581.5:c.1657A>T
|
ENSP00000440252.1:p.Ser553Cys
|
|
ENST00000559816.1:n.1500A>T
|
|
|
NM_001306146.1:c.1657A>T
|
NP_001293075.1:p.Ser553Cys
|
|
NM_002112.3:c.1756A>T
|
NP_002103.2:p.Ser586Cys
|
|
XM_011521479.1:c.1519A>T
|
XP_011519781.1:p.Ser507Cys
|
|
XM_011521480.1:c.1324A>T
|
XP_011519782.1:p.Ser442Cys
|
|
XM_017022094.1:c.1861A>T
|
XP_016877583.1:p.Ser621Cys
|
|
XM_017022095.1:c.1762A>T
|
XP_016877584.1:p.Ser588Cys
|
|
XM_017022096.1:c.1633A>T
|
XP_016877585.1:p.Ser545Cys
|
|
XM_017022097.1:c.1624A>T
|
XP_016877586.1:p.Ser542Cys
|
|
XM_017022098.1:c.1429A>T
|
XP_016877587.1:p.Ser477Cys
|
|
NM_002112.4:c.1756A>T
MANE Select
|
NP_002103.2:p.Ser586Cys
|
|
NM_001306146.2:c.1657A>T
|
NP_001293075.1:p.Ser553Cys
|
|