ENST00000220616.9:c.8164A>T
MANE Select
|
ENSP00000220616.4:p.Ile2722Phe
|
|
ENST00000220616.8:c.8164A>T
|
ENSP00000220616.4:p.Ile2722Phe
|
|
ENST00000519178.5:c.3530A>T
|
|
|
ENST00000519543.5:c.2563A>T
|
ENSP00000430430.1:p.Ile855Phe
|
|
ENST00000521107.1:c.376A>T
|
ENSP00000430161.1:p.Ile126Phe
|
|
ENST00000522691.1:n.250A>T
|
|
|
ENST00000523756.5:c.4819A>T
|
|
|
NM_003235.4:c.8164A>T
|
NP_003226.4:p.Ile2722Phe
|
|
XM_005251038.3:c.7972A>T
|
XP_005251095.1:p.Ile2658Phe
|
|
XM_006716622.2:c.8101A>T
|
XP_006716685.1:p.Ile2701Phe
|
|
XM_005251038.4:c.7972A>T
|
XP_005251095.1:p.Ile2658Phe
|
|
XM_006716622.3:c.8101A>T
|
XP_006716685.1:p.Ile2701Phe
|
|
XM_017013793.1:c.8098A>T
|
XP_016869282.1:p.Ile2700Phe
|
|
XM_017013794.1:c.8029A>T
|
XP_016869283.1:p.Ile2677Phe
|
|
XM_017013795.1:c.7993A>T
|
XP_016869284.1:p.Ile2665Phe
|
|
XM_017013796.1:c.7945A>T
|
XP_016869285.1:p.Ile2649Phe
|
|
XM_017013797.1:c.7903A>T
|
XP_016869286.1:p.Ile2635Phe
|
|
NM_003235.5:c.8164A>T
MANE Select
|
NP_003226.4:p.Ile2722Phe
|
|