|
ENST00000561793.2:c.369G>T
|
|
|
|
ENST00000564213.2:c.1100G>T
|
ENSP00000518583.1:p.Gly367Val
|
|
|
ENST00000565665.6:n.1473G>T
|
|
|
|
ENST00000567203.2:n.1215G>T
|
|
|
|
ENST00000711102.1:c.1100G>T
|
ENSP00000518580.1:p.Gly367Val
|
|
|
ENST00000711103.1:c.1100G>T
|
ENSP00000518581.1:p.Gly367Val
|
|
|
ENST00000711104.1:c.1151G>T
|
ENSP00000518582.1:p.Gly384Val
|
|
|
ENST00000711105.1:c.1100G>T
|
ENSP00000518584.1:p.Gly367Val
|
|
|
ENST00000711111.1:n.1216G>T
|
|
|
|
ENST00000426824.8:c.1100G>T
MANE Select
|
ENSP00000407242.4:p.Gly367Val
|
|
|
ENST00000324385.9:c.1205G>T
|
ENSP00000324510.5:p.Gly402Val
|
|
|
ENST00000397488.6:c.1151G>T
|
ENSP00000380625.2:p.Gly384Val
|
|
|
ENST00000421665.6:c.992G>T
|
ENSP00000409533.2:p.Gly331Val
|
|
|
ENST00000426824.7:c.1100G>T
|
ENSP00000407242.3:p.Gly367Val
|
|
|
ENST00000562208.5:c.1031G>T
|
ENSP00000458134.1:p.Gly344Val
|
|
|
ENST00000568887.5:c.1016G>T
|
ENSP00000457644.1:p.Gly339Val
|
|
|
ENST00000628027.2:c.1151G>T
|
ENSP00000487275.1:p.Gly384Val
|
|
|
NM_001199096.1:c.992G>T
|
NP_001186025.1:p.Gly331Val
|
|
|
NM_001199097.1:c.1100G>T
|
NP_001186026.1:p.Gly367Val
|
|
|
NM_001199098.1:c.1031G>T
|
NP_001186027.1:p.Gly344Val
|
|
|
NM_001199099.1:c.1016G>T
|
NP_001186028.1:p.Gly339Val
|
|
|
NM_001286464.1:c.1151G>T
|
NP_001273393.1:p.Gly384Val
|
|
|
NM_003933.4:c.1205G>T
|
NP_003924.2:p.Gly402Val
|
|
|
XM_011522728.1:c.1256G>T
|
XP_011521030.1:p.Gly419Val
|
|
|
XM_011522729.1:c.1256G>T
|
XP_011521031.1:p.Gly419Val
|
|
|
XM_011522730.1:c.1256G>T
|
XP_011521032.1:p.Gly419Val
|
|
|
XM_011522730.2:c.1256G>T
|
XP_011521032.1:p.Gly419Val
|
|
|
NM_001199097.2:c.1100G>T
MANE Select
|
NP_001186026.1:p.Gly367Val
|
|
|
NM_001199098.2:c.1031G>T
|
NP_001186027.1:p.Gly344Val
|
|
|
NM_001199099.2:c.1016G>T
|
NP_001186028.1:p.Gly339Val
|
|
|
NM_001286464.2:c.1151G>T
|
NP_001273393.2:p.Gly384Val
|
|
|
NM_001199096.2:c.992G>T
|
NP_001186025.1:p.Gly331Val
|
|
|
NM_003933.5:c.1205G>T
|
NP_003924.2:p.Gly402Val
|
|
