ENST00000395925.8:c.2986G>C
MANE Select
|
ENSP00000379258.3:p.Asp996His
|
|
ENST00000677288.1:c.2812G>C
|
ENSP00000503986.1:p.Asp938His
|
|
ENST00000677605.1:c.2986G>C
|
ENSP00000503743.1:p.Asp996His
|
|
ENST00000678429.1:c.2986G>C
|
ENSP00000502957.1:p.Asp996His
|
|
ENST00000395925.7:c.2986G>C
|
ENSP00000379258.3:p.Asp996His
|
|
ENST00000479210.1:n.2963G>C
|
|
|
NM_000168.5:c.2986G>C
|
NP_000159.3:p.Asp996His
|
|
XM_005249703.1:c.2986G>C
|
XP_005249760.1:p.Asp996His
|
|
XM_005249704.2:c.2986G>C
|
XP_005249761.1:p.Asp996His
|
|
XM_011515272.1:c.2986G>C
|
XP_011513574.1:p.Asp996His
|
|
XM_011515273.1:c.2986G>C
|
XP_011513575.1:p.Asp996His
|
|
XM_011515274.1:c.2809G>C
|
XP_011513576.1:p.Asp937His
|
|
XM_011515274.2:c.2809G>C
|
XP_011513576.1:p.Asp937His
|
|
XM_017011997.1:c.2983G>C
|
XP_016867486.1:p.Asp995His
|
|
NM_000168.6:c.2986G>C
MANE Select
|
NP_000159.3:p.Asp996His
|
|