|
ENST00000359206.8:c.1865G>T
|
ENSP00000352135.3:p.Gly622Val
|
|
|
ENST00000643670.1:c.1881G>T
|
ENSP00000496629.1:n.1881G>T
|
|
|
ENST00000644106.1:c.*1402G>T
|
ENSP00000493477.1:n.*1402G>T
|
|
|
ENST00000649586.2:c.1865G>T
MANE Select
|
ENSP00000496956.2:p.Gly622Val
|
|
|
ENST00000265723.8:c.1865G>T
|
ENSP00000265723.4:p.Gly622Val
|
|
|
ENST00000358400.7:c.1865G>T
|
ENSP00000351172.3:p.Gly622Val
|
|
|
ENST00000359206.7:c.1865G>T
|
ENSP00000352135.3:p.Gly622Val
|
|
|
ENST00000453593.5:c.1865G>T
|
ENSP00000392983.1:p.Gly622Val
|
|
|
ENST00000469770.1:n.69G>T
|
|
|
|
NM_000443.3:c.1865G>T
|
NP_000434.1:p.Gly622Val
|
|
|
NM_018849.2:c.1865G>T
|
NP_061337.1:p.Gly622Val
|
|
|
NM_018850.2:c.1865G>T
|
NP_061338.1:p.Gly622Val
|
|
|
XM_011516308.1:c.1865G>T
|
XP_011514610.1:p.Gly622Val
|
|
|
XM_011516309.1:c.1865G>T
|
XP_011514611.1:p.Gly622Val
|
|
|
XM_011516310.1:c.1865G>T
|
XP_011514612.1:p.Gly622Val
|
|
|
XM_011516311.1:c.1865G>T
|
XP_011514613.1:p.Gly622Val
|
|
|
XM_011516312.1:c.1865G>T
|
XP_011514614.1:p.Gly622Val
|
|
|
XM_011516313.1:c.1865G>T
|
XP_011514615.1:p.Gly622Val
|
|
|
XM_011516314.1:c.1886G>T
|
XP_011514616.1:p.Gly629Val
|
|
|
XM_011516315.1:c.1205G>T
|
XP_011514617.1:p.Gly402Val
|
|
|
XR_927478.1:n.1961G>T
|
|
|
|
XM_011516308.3:c.2135G>T
|
XP_011514610.3:p.Gly712Val
|
|
|
XM_011516309.3:c.2135G>T
|
XP_011514611.3:p.Gly712Val
|
|
|
XM_011516310.3:c.2135G>T
|
XP_011514612.3:p.Gly712Val
|
|
|
XM_011516311.3:c.2135G>T
|
XP_011514613.3:p.Gly712Val
|
|
|
XM_011516312.3:c.2135G>T
|
XP_011514614.3:p.Gly712Val
|
|
|
XM_011516313.3:c.2135G>T
|
XP_011514615.2:p.Gly712Val
|
|
|
XM_011516315.3:c.1205G>T
|
XP_011514617.2:p.Gly402Val
|
|
|
XM_017012323.2:c.1865G>T
|
XP_016867812.1:p.Gly622Val
|
|
|
XR_001744809.2:n.2636G>T
|
|
|
|
XR_001744810.2:n.2631G>T
|
|
|
|
NM_000443.4:c.1865G>T
MANE Select
|
NP_000434.1:p.Gly622Val
|
|
|
NM_018849.3:c.1865G>T
|
NP_061337.1:p.Gly622Val
|
|
|
NM_018850.3:c.1865G>T
|
NP_061338.1:p.Gly622Val
|
|
