|
NM_001754.5:c.832C>T
MANE Select
|
NP_001745.2:p.Pro278Ser
|
|
ENST00000675419.1:c.832C>T
MANE Select
|
ENSP00000501943.1:p.Pro278Ser
|
|
NM_001001890.2:c.751C>T
|
NP_001001890.1:p.Pro251Ser
|
|
NM_001001890.3:c.751C>T
|
NP_001001890.1:p.Pro251Ser
|
|
NM_001754.4:c.832C>T , LRG_482t1:c.832C>T
|
NP_001745.2:p.Pro278Ser
|
|
ENST00000300305.7:c.832C>T
|
ENSP00000300305.3:p.Pro278Ser
|
|
ENST00000344691.8:c.751C>T
|
ENSP00000340690.4:p.Pro251Ser
|
|
ENST00000399240.5:c.559C>T
|
ENSP00000382184.1:p.Pro187Ser
|
|
ENST00000437180.5:c.832C>T
|
ENSP00000409227.1:p.Pro278Ser
|
|
ENST00000482318.5:c.*422C>T
|
ENSP00000477067.1:n.*422C>T
|
|
XM_005261068.3:c.796C>T
|
XP_005261125.1:p.Pro266Ser
|
|
XM_005261069.3:c.640C>T
|
XP_005261126.1:p.Pro214Ser
|
|
XM_005261069.4:c.640C>T
|
XP_005261126.1:p.Pro214Ser
|
|
XM_011529766.1:c.832C>T
|
XP_011528068.1:p.Pro278Ser
|
|
XM_011529766.2:c.832C>T
|
XP_011528068.1:p.Pro278Ser
|
|
XM_011529767.1:c.793C>T
|
XP_011528069.1:p.Pro265Ser
|
|
XM_011529767.2:c.793C>T
|
XP_011528069.1:p.Pro265Ser
|
|
XM_011529768.1:c.601C>T
|
XP_011528070.1:p.Pro201Ser
|
|
XM_011529768.2:c.601C>T
|
XP_011528070.1:p.Pro201Ser
|
|
XM_017028487.1:c.679C>T
|
XP_016883976.1:p.Pro227Ser
|
|
XR_937576.1:n.1011C>T
|
|
|
XR_937576.2:n.1058C>T
|
|
