ENST00000220616.9:c.8153G>C
MANE Select
|
ENSP00000220616.4:p.Trp2718Ser
|
|
ENST00000220616.8:c.8153G>C
|
ENSP00000220616.4:p.Trp2718Ser
|
|
ENST00000519178.5:c.3519G>C
|
|
|
ENST00000519543.5:c.2552G>C
|
ENSP00000430430.1:p.Trp851Ser
|
|
ENST00000521107.1:c.365G>C
|
ENSP00000430161.1:p.Trp122Ser
|
|
ENST00000522691.1:n.239G>C
|
|
|
ENST00000523756.5:c.4808G>C
|
|
|
NM_003235.4:c.8153G>C
|
NP_003226.4:p.Trp2718Ser
|
|
XM_005251038.3:c.7961G>C
|
XP_005251095.1:p.Trp2654Ser
|
|
XM_006716622.2:c.8090G>C
|
XP_006716685.1:p.Trp2697Ser
|
|
XM_005251038.4:c.7961G>C
|
XP_005251095.1:p.Trp2654Ser
|
|
XM_006716622.3:c.8090G>C
|
XP_006716685.1:p.Trp2697Ser
|
|
XM_017013793.1:c.8087G>C
|
XP_016869282.1:p.Trp2696Ser
|
|
XM_017013794.1:c.8018G>C
|
XP_016869283.1:p.Trp2673Ser
|
|
XM_017013795.1:c.7982G>C
|
XP_016869284.1:p.Trp2661Ser
|
|
XM_017013796.1:c.7934G>C
|
XP_016869285.1:p.Trp2645Ser
|
|
XM_017013797.1:c.7892G>C
|
XP_016869286.1:p.Trp2631Ser
|
|
NM_003235.5:c.8153G>C
MANE Select
|
NP_003226.4:p.Trp2718Ser
|
|