ENST00000359206.8:c.3743G>T
|
ENSP00000352135.3:p.Gly1248Val
|
|
ENST00000649586.2:c.3743G>T
MANE Select
|
ENSP00000496956.2:p.Gly1248Val
|
|
ENST00000265723.8:c.3764G>T
|
ENSP00000265723.4:p.Gly1255Val
|
|
ENST00000358400.7:c.3602G>T
|
ENSP00000351172.3:p.Gly1201Val
|
|
ENST00000359206.7:c.3743G>T
|
ENSP00000352135.3:p.Gly1248Val
|
|
ENST00000440025.1:c.177G>T
|
|
|
ENST00000453593.5:c.3602G>T
|
ENSP00000392983.1:p.Gly1201Val
|
|
ENST00000467983.1:n.355G>T
|
|
|
NM_000443.3:c.3743G>T
|
NP_000434.1:p.Gly1248Val
|
|
NM_018849.2:c.3764G>T
|
NP_061337.1:p.Gly1255Val
|
|
NM_018850.2:c.3602G>T
|
NP_061338.1:p.Gly1201Val
|
|
XM_011516308.1:c.3764G>T
|
XP_011514610.1:p.Gly1255Val
|
|
XM_011516309.1:c.3743G>T
|
XP_011514611.1:p.Gly1248Val
|
|
XM_011516310.1:c.3659G>T
|
XP_011514612.1:p.Gly1220Val
|
|
XM_011516311.1:c.3635G>T
|
XP_011514613.1:p.Gly1212Val
|
|
XM_011516312.1:c.3623G>T
|
XP_011514614.1:p.Gly1208Val
|
|
XM_011516313.1:c.3602G>T
|
XP_011514615.1:p.Gly1201Val
|
|
XM_011516314.1:c.3785G>T
|
XP_011514616.1:p.Gly1262Val
|
|
XM_011516315.1:c.3104G>T
|
XP_011514617.1:p.Gly1035Val
|
|
XM_011516308.3:c.4034G>T
|
XP_011514610.3:p.Gly1345Val
|
|
XM_011516309.3:c.4013G>T
|
XP_011514611.3:p.Gly1338Val
|
|
XM_011516310.3:c.3929G>T
|
XP_011514612.3:p.Gly1310Val
|
|
XM_011516311.3:c.3905G>T
|
XP_011514613.3:p.Gly1302Val
|
|
XM_011516312.3:c.3893G>T
|
XP_011514614.3:p.Gly1298Val
|
|
XM_011516313.3:c.3872G>T
|
XP_011514615.2:p.Gly1291Val
|
|
XM_011516315.3:c.3104G>T
|
XP_011514617.2:p.Gly1035Val
|
|
XM_017012323.2:c.3764G>T
|
XP_016867812.1:p.Gly1255Val
|
|
XR_001744809.2:n.4272G>T
|
|
|
NM_000443.4:c.3743G>T
MANE Select
|
NP_000434.1:p.Gly1248Val
|
|
NM_018849.3:c.3764G>T
|
NP_061337.1:p.Gly1255Val
|
|
NM_018850.3:c.3602G>T
|
NP_061338.1:p.Gly1201Val
|
|