ENST00000525341.2:c.634G>T
|
|
|
ENST00000528641.7:c.468G>T
|
ENSP00000434982.3:p.Gly156=
|
|
ENST00000529797.2:n.1169G>T
|
|
|
ENST00000682324.1:c.469-670G>T
|
ENSP00000508017.1:n.469-670G>T
|
|
ENST00000682659.1:c.288G>T
|
ENSP00000507351.1:p.Gly96=
|
|
ENST00000682699.1:c.657G>T
|
ENSP00000507935.1:p.Gly219=
|
|
ENST00000683237.1:c.657G>T
|
ENSP00000507343.1:p.Gly219=
|
|
ENST00000683856.1:c.480G>T
|
ENSP00000507979.1:p.Gly160=
|
|
ENST00000684006.1:c.657G>T
|
ENSP00000507269.1:p.Gly219=
|
|
ENST00000684657.1:c.477G>T
|
ENSP00000507961.1:p.Gly159=
|
|
ENST00000279146.8:c.657G>T
MANE Select
|
ENSP00000279146.3:p.Gly219=
|
|
ENST00000279146.7:c.657G>T
|
ENSP00000279146.3:p.Gly219=
|
|
ENST00000525341.1:c.309G>T
|
ENSP00000476993.1:p.Gly103=
|
|
ENST00000528641.6:c.468G>T
|
ENSP00000434982.2:p.Gly156=
|
|
NM_001302959.1:c.480G>T
|
NP_001289888.1:p.Gly160=
|
|
NM_001302960.1:c.657G>T
|
NP_001289889.1:p.Gly219=
|
|
NM_003977.3:c.657G>T
|
NP_003968.3:p.Gly219=
|
|
XM_024448761.1:c.657G>T
|
XP_024304529.1:p.Gly219=
|
|
NM_003977.4:c.657G>T
MANE Select
|
NP_003968.3:p.Gly219=
|
|
NM_001302960.2:c.657G>T
|
NP_001289889.1:p.Gly219=
|
|
NM_001302959.2:c.480G>T
|
NP_001289888.1:p.Gly160=
|
|