ENST00000220616.9:c.8016T>C
MANE Select
|
ENSP00000220616.4:p.Tyr2672=
|
|
ENST00000220616.8:c.8016T>C
|
ENSP00000220616.4:p.Tyr2672=
|
|
ENST00000519178.5:c.3382T>C
|
|
|
ENST00000519543.5:c.2415T>C
|
ENSP00000430430.1:p.Tyr805=
|
|
ENST00000521107.1:c.228T>C
|
ENSP00000430161.1:p.Tyr76=
|
|
ENST00000522691.1:n.102T>C
|
|
|
ENST00000523756.5:c.4671T>C
|
|
|
NM_003235.4:c.8016T>C
|
NP_003226.4:p.Tyr2672=
|
|
XM_005251038.3:c.7824T>C
|
XP_005251095.1:p.Tyr2608=
|
|
XM_006716622.2:c.7953T>C
|
XP_006716685.1:p.Tyr2651=
|
|
XM_005251038.4:c.7824T>C
|
XP_005251095.1:p.Tyr2608=
|
|
XM_006716622.3:c.7953T>C
|
XP_006716685.1:p.Tyr2651=
|
|
XM_017013793.1:c.7950T>C
|
XP_016869282.1:p.Tyr2650=
|
|
XM_017013794.1:c.7881T>C
|
XP_016869283.1:p.Tyr2627=
|
|
XM_017013795.1:c.7845T>C
|
XP_016869284.1:p.Tyr2615=
|
|
XM_017013796.1:c.7797T>C
|
XP_016869285.1:p.Tyr2599=
|
|
XM_017013797.1:c.7755T>C
|
XP_016869286.1:p.Tyr2585=
|
|
NM_003235.5:c.8016T>C
MANE Select
|
NP_003226.4:p.Tyr2672=
|
|