ENST00000220616.9:c.8162A>C
MANE Select
|
ENSP00000220616.4:p.Tyr2721Ser
|
|
ENST00000220616.8:c.8162A>C
|
ENSP00000220616.4:p.Tyr2721Ser
|
|
ENST00000519178.5:c.3528A>C
|
|
|
ENST00000519543.5:c.2561A>C
|
ENSP00000430430.1:p.Tyr854Ser
|
|
ENST00000521107.1:c.374A>C
|
ENSP00000430161.1:p.Tyr125Ser
|
|
ENST00000522691.1:n.248A>C
|
|
|
ENST00000523756.5:c.4817A>C
|
|
|
NM_003235.4:c.8162A>C
|
NP_003226.4:p.Tyr2721Ser
|
|
XM_005251038.3:c.7970A>C
|
XP_005251095.1:p.Tyr2657Ser
|
|
XM_006716622.2:c.8099A>C
|
XP_006716685.1:p.Tyr2700Ser
|
|
XM_005251038.4:c.7970A>C
|
XP_005251095.1:p.Tyr2657Ser
|
|
XM_006716622.3:c.8099A>C
|
XP_006716685.1:p.Tyr2700Ser
|
|
XM_017013793.1:c.8096A>C
|
XP_016869282.1:p.Tyr2699Ser
|
|
XM_017013794.1:c.8027A>C
|
XP_016869283.1:p.Tyr2676Ser
|
|
XM_017013795.1:c.7991A>C
|
XP_016869284.1:p.Tyr2664Ser
|
|
XM_017013796.1:c.7943A>C
|
XP_016869285.1:p.Tyr2648Ser
|
|
XM_017013797.1:c.7901A>C
|
XP_016869286.1:p.Tyr2634Ser
|
|
NM_003235.5:c.8162A>C
MANE Select
|
NP_003226.4:p.Tyr2721Ser
|
|