ENST00000461280.2:n.1372C>A
|
|
|
ENST00000683359.1:n.198C>A
|
|
|
ENST00000684241.1:n.2907C>A
|
|
|
ENST00000262186.10:c.2074C>A
MANE Select
|
ENSP00000262186.5:p.Pro692Thr
|
|
ENST00000330883.9:c.1054C>A
|
ENSP00000328531.4:p.Pro352Thr
|
|
ENST00000262186.9:c.2074C>A
|
ENSP00000262186.5:p.Pro692Thr
|
|
ENST00000330883.8:c.1054C>A
|
ENSP00000328531.4:p.Pro352Thr
|
|
ENST00000430723.4:c.1726C>A
|
ENSP00000387657.4:p.Pro576Thr
|
|
ENST00000461280.1:n.1361C>A
|
|
|
ENST00000473610.5:n.1706C>A
|
|
|
ENST00000532957.5:n.2297C>A
|
|
|
NM_000238.3:c.2074C>A , LRG_288t1:c.2074C>A
|
NP_000229.1:p.Pro692Thr
|
|
NM_001204798.1:c.1054C>A
|
NP_001191727.1:p.Pro352Thr
|
|
NM_172056.2:c.2074C>A , LRG_288t2:c.2074C>A
|
NP_742053.1:p.Pro692Thr
|
|
NM_172057.2:c.1054C>A , LRG_288t3:c.1054C>A
|
NP_742054.1:p.Pro352Thr
|
|
XM_011516185.1:c.1774C>A
|
XP_011514487.1:p.Pro592Thr
|
|
XM_011516186.1:c.2074C>A
|
XP_011514488.1:p.Pro692Thr
|
|
XM_011516185.2:c.1774C>A
|
XP_011514487.1:p.Pro592Thr
|
|
XM_011516186.3:c.2074C>A
|
XP_011514488.1:p.Pro692Thr
|
|
XM_017012195.1:c.1924C>A
|
XP_016867684.1:p.Pro642Thr
|
|
XM_017012196.1:c.1897C>A
|
XP_016867685.1:p.Pro633Thr
|
|
NM_000238.4:c.2074C>A
MANE Select
|
NP_000229.1:p.Pro692Thr
|
|
NM_001204798.2:c.1054C>A
|
NP_001191727.1:p.Pro352Thr
|
|
NM_172057.3:c.1054C>A
|
NP_742054.1:p.Pro352Thr
|
|