|
ENST00000466617.6:c.701G>T
|
ENSP00000420082.2:p.Gly234Val
|
|
|
ENST00000470367.2:c.989G>T
|
ENSP00000514541.1:p.Gly330Val
|
|
|
ENST00000483566.2:c.701G>T
|
ENSP00000420252.2:p.Gly234Val
|
|
|
ENST00000699714.1:c.701G>T
|
ENSP00000514539.1:p.Gly234Val
|
|
|
ENST00000699715.1:c.701G>T
|
ENSP00000514540.1:p.Gly234Val
|
|
|
ENST00000699716.1:c.701G>T
|
ENSP00000514542.1:p.Gly234Val
|
|
|
ENST00000699718.1:c.2024G>T
|
ENSP00000514543.1:p.Gly675Val
|
|
|
ENST00000699719.1:n.283G>T
|
|
|
|
ENST00000462833.6:c.2024G>T
MANE Select
|
ENSP00000419361.1:p.Gly675Val
|
|
|
ENST00000309879.9:c.974G>T
|
ENSP00000308685.5:p.Gly325Val
|
|
|
ENST00000462833.5:c.2024G>T
|
ENSP00000419361.1:p.Gly675Val
|
|
|
ENST00000466617.5:c.701G>T
|
ENSP00000420082.1:p.Gly234Val
|
|
|
ENST00000491190.5:c.923G>T
|
ENSP00000418537.1:p.Gly308Val
|
|
|
NM_001199642.1:c.974G>T
|
NP_001186571.1:p.Gly325Val
|
|
|
NM_183357.2:c.2024G>T
|
NP_899200.1:p.Gly675Val
|
|
|
XM_005247077.2:c.2024G>T
|
XP_005247134.1:p.Gly675Val
|
|
|
XM_005247078.1:c.974G>T
|
XP_005247135.1:p.Gly325Val
|
|
|
XM_006713483.1:c.923G>T
|
XP_006713546.1:p.Gly308Val
|
|
|
XM_006713484.1:c.701G>T
|
XP_006713547.1:p.Gly234Val
|
|
|
XM_011512358.1:c.2024G>T
|
XP_011510660.1:p.Gly675Val
|
|
|
XM_011512359.1:c.1025G>T
|
XP_011510661.1:p.Gly342Val
|
|
|
XM_011512360.1:c.935G>T
|
XP_011510662.1:p.Gly312Val
|
|
|
XM_011512361.1:c.701G>T
|
XP_011510663.1:p.Gly234Val
|
|
|
XM_005247077.4:c.2024G>T
|
XP_005247134.1:p.Gly675Val
|
|
|
XM_011512359.2:c.1025G>T
|
XP_011510661.1:p.Gly342Val
|
|
|
XM_011512360.3:c.935G>T
|
XP_011510662.1:p.Gly312Val
|
|
|
XM_017005638.1:c.926G>T
|
XP_016861127.1:p.Gly309Val
|
|
|
XM_017005639.1:c.926G>T
|
XP_016861128.1:p.Gly309Val
|
|
|
NM_001378259.1:c.2024G>T
|
NP_001365188.1:p.Gly675Val
|
|
|
NM_183357.3:c.2024G>T
MANE Select
|
NP_899200.1:p.Gly675Val
|
|
