ENST00000558739.2:c.191G>T
|
ENSP00000453684.2:p.Gly64Val
|
|
ENST00000559460.6:c.191G>T
|
ENSP00000453082.2:p.Gly64Val
|
|
ENST00000560424.2:c.506G>T
|
ENSP00000455540.2:p.Gly169Val
|
|
ENST00000327367.9:c.506G>T
MANE Select
|
ENSP00000332973.4:p.Gly169Val
|
|
ENST00000679624.1:c.191G>T
|
ENSP00000505445.1:p.Gly64Val
|
|
ENST00000681239.1:c.191G>T
|
ENSP00000505641.1:p.Gly64Val
|
|
ENST00000327367.8:c.506G>T
|
ENSP00000332973.4:p.Gly169Val
|
|
ENST00000439724.7:c.374G>T
|
ENSP00000401133.3:p.Gly125Val
|
|
ENST00000540846.6:c.191G>T
|
ENSP00000437757.2:p.Gly64Val
|
|
ENST00000558894.5:c.191G>T
|
ENSP00000458060.1:p.Gly64Val
|
|
ENST00000559460.5:c.191G>T
|
ENSP00000453082.1:p.Gly64Val
|
|
ENST00000559937.1:n.356G>T
|
|
|
ENST00000560175.5:c.191G>T
|
ENSP00000455095.1:p.Gly64Val
|
|
NM_001145102.1:c.191G>T
|
NP_001138574.1:p.Gly64Val
|
|
NM_001145103.1:c.374G>T
|
NP_001138575.1:p.Gly125Val
|
|
NM_005902.3:c.506G>T
|
NP_005893.1:p.Gly169Val
|
|
XM_011521559.1:c.400+270G>T
|
XP_011519861.1:n.400+270G>T
|
|
XM_011521560.1:c.359G>T
|
XP_011519862.1:p.Gly120Val
|
|
XM_011521559.3:c.400+270G>T
|
XP_011519861.1:n.400+270G>T
|
|
NM_005902.4:c.506G>T
MANE Select
|
NP_005893.1:p.Gly169Val
|
|
NM_001145102.2:c.191G>T
|
NP_001138574.1:p.Gly64Val
|
|
NM_001145103.2:c.374G>T
|
NP_001138575.1:p.Gly125Val
|
|