ENST00000267845.8:c.1829C>A
MANE Select
|
ENSP00000267845.3:p.Ser610Tyr
|
|
ENST00000267845.7:c.1829C>A
|
ENSP00000267845.3:p.Ser610Tyr
|
|
ENST00000543581.5:c.1730C>A
|
ENSP00000440252.1:p.Ser577Tyr
|
|
ENST00000559816.1:n.1573C>A
|
|
|
NM_001306146.1:c.1730C>A
|
NP_001293075.1:p.Ser577Tyr
|
|
NM_002112.3:c.1829C>A
|
NP_002103.2:p.Ser610Tyr
|
|
XM_011521479.1:c.1592C>A
|
XP_011519781.1:p.Ser531Tyr
|
|
XM_011521480.1:c.1397C>A
|
XP_011519782.1:p.Ser466Tyr
|
|
XM_017022094.1:c.1934C>A
|
XP_016877583.1:p.Ser645Tyr
|
|
XM_017022095.1:c.1835C>A
|
XP_016877584.1:p.Ser612Tyr
|
|
XM_017022096.1:c.1706C>A
|
XP_016877585.1:p.Ser569Tyr
|
|
XM_017022097.1:c.1697C>A
|
XP_016877586.1:p.Ser566Tyr
|
|
XM_017022098.1:c.1502C>A
|
XP_016877587.1:p.Ser501Tyr
|
|
NM_002112.4:c.1829C>A
MANE Select
|
NP_002103.2:p.Ser610Tyr
|
|
NM_001306146.2:c.1730C>A
|
NP_001293075.1:p.Ser577Tyr
|
|