ENST00000267845.8:c.1771C>T
MANE Select
|
ENSP00000267845.3:p.Pro591Ser
|
|
ENST00000267845.7:c.1771C>T
|
ENSP00000267845.3:p.Pro591Ser
|
|
ENST00000543581.5:c.1672C>T
|
ENSP00000440252.1:p.Pro558Ser
|
|
ENST00000559816.1:n.1515C>T
|
|
|
NM_001306146.1:c.1672C>T
|
NP_001293075.1:p.Pro558Ser
|
|
NM_002112.3:c.1771C>T
|
NP_002103.2:p.Pro591Ser
|
|
XM_011521479.1:c.1534C>T
|
XP_011519781.1:p.Pro512Ser
|
|
XM_011521480.1:c.1339C>T
|
XP_011519782.1:p.Pro447Ser
|
|
XM_017022094.1:c.1876C>T
|
XP_016877583.1:p.Pro626Ser
|
|
XM_017022095.1:c.1777C>T
|
XP_016877584.1:p.Pro593Ser
|
|
XM_017022096.1:c.1648C>T
|
XP_016877585.1:p.Pro550Ser
|
|
XM_017022097.1:c.1639C>T
|
XP_016877586.1:p.Pro547Ser
|
|
XM_017022098.1:c.1444C>T
|
XP_016877587.1:p.Pro482Ser
|
|
NM_002112.4:c.1771C>T
MANE Select
|
NP_002103.2:p.Pro591Ser
|
|
NM_001306146.2:c.1672C>T
|
NP_001293075.1:p.Pro558Ser
|
|