ENST00000651372.2:c.10590T>C
MANE Select
|
ENSP00000498627.1:p.Leu3530=
|
|
ENST00000518282.5:c.10512T>C
|
ENSP00000430848.1:p.Leu3504=
|
|
ENST00000521891.6:c.10590T>C
|
ENSP00000430497.2:p.Leu3530=
|
|
NM_024721.4:c.10590T>C
|
NP_078997.4:p.Leu3530=
|
|
XM_011517592.1:c.10590T>C
|
XP_011515894.1:p.Leu3530=
|
|
XM_011517593.1:c.10590T>C
|
XP_011515895.1:p.Leu3530=
|
|
XM_011517594.1:c.10590T>C
|
XP_011515896.1:p.Leu3530=
|
|
XM_011517595.1:c.10590T>C
|
XP_011515897.1:p.Leu3530=
|
|
XM_011517596.1:c.10512T>C
|
XP_011515898.1:p.Leu3504=
|
|
XM_011517597.1:c.10473T>C
|
XP_011515899.1:p.Leu3491=
|
|
XM_011517592.3:c.10590T>C
|
XP_011515894.1:p.Leu3530=
|
|
XM_011517593.2:c.10590T>C
|
XP_011515895.1:p.Leu3530=
|
|
XM_011517594.2:c.10590T>C
|
XP_011515896.1:p.Leu3530=
|
|
XM_011517595.2:c.10590T>C
|
XP_011515897.1:p.Leu3530=
|
|
XM_011517596.2:c.10512T>C
|
XP_011515898.1:p.Leu3504=
|
|
XM_011517597.2:c.10473T>C
|
XP_011515899.1:p.Leu3491=
|
|
XM_017013845.1:c.10395T>C
|
XP_016869334.1:p.Leu3465=
|
|
NM_024721.5:c.10590T>C
MANE Select
|
NP_078997.4:p.Leu3530=
|
|