ENST00000466474.6:c.196G>T
|
ENSP00000511987.1:p.Gly66Ter
|
|
ENST00000695525.1:n.282G>T
|
|
|
ENST00000695526.1:c.196G>T
|
ENSP00000511988.1:p.Gly66Ter
|
|
ENST00000695558.1:c.196G>T
|
ENSP00000512015.1:p.Gly66Ter
|
|
ENST00000703224.1:c.196G>T
|
ENSP00000515242.1:p.Gly66Ter
|
|
ENST00000703225.1:n.1631G>T
|
|
|
ENST00000359568.10:c.196G>T
MANE Select
|
ENSP00000352572.5:p.Gly66Ter
|
|
ENST00000359568.9:c.196G>T
|
ENSP00000352572.5:p.Gly66Ter
|
|
ENST00000480896.5:n.465G>T
|
|
|
ENST00000490468.5:n.284G>T
|
|
|
NM_001315529.1:c.-159G>T
|
NP_001302458.1:n.-159G>T
|
|
NM_006031.5:c.196G>T
|
NP_006022.3:p.Gly66Ter
|
|
XM_005261124.3:c.196G>T
|
XP_005261181.1:p.Gly66Ter
|
|
XM_011529593.1:c.196G>T
|
XP_011527895.1:p.Gly66Ter
|
|
XM_011529594.1:c.196G>T
|
XP_011527896.1:p.Gly66Ter
|
|
XM_005261124.5:c.196G>T
|
XP_005261181.1:p.Gly66Ter
|
|
XM_011529594.3:c.196G>T
|
XP_011527896.1:p.Gly66Ter
|
|
XM_017028362.2:c.196G>T
|
XP_016883851.1:p.Gly66Ter
|
|
XM_017028363.1:c.-159G>T
|
XP_016883852.1:n.-159G>T
|
|
XM_024452083.1:c.-1913G>T
|
XP_024307851.1:n.-1913G>T
|
|
NM_006031.6:c.196G>T
MANE Select
|
NP_006022.3:p.Gly66Ter
|
|
NM_001315529.2:c.-159G>T
|
NP_001302458.1:n.-159G>T
|
|