ENST00000529510.6:n.1048G>A
|
|
|
ENST00000697845.1:n.1828G>A
|
|
|
ENST00000697846.1:n.1048G>A
|
|
|
ENST00000697847.1:n.1202-290G>A
|
|
|
ENST00000697848.1:n.1134G>A
|
|
|
ENST00000697849.1:n.2943G>A
|
|
|
ENST00000697850.1:n.1134G>A
|
|
|
ENST00000697851.1:n.2742G>A
|
|
|
ENST00000638186.1:n.1208G>A
|
|
|
ENST00000638360.1:n.1040G>A
|
|
|
ENST00000638925.1:n.1173G>A
|
|
|
ENST00000650539.1:n.1310G>A
|
|
|
ENST00000330775.9:c.904G>A
|
ENSP00000476242.2:p.Gly302Ser
|
|
ENST00000357590.9:c.904G>A
|
ENSP00000476176.2:p.Gly302Ser
|
|
ENST00000524428.5:n.1140G>A
|
|
|
ENST00000525039.5:n.1328G>A
|
|
|
ENST00000525102.5:n.1662G>A
|
|
|
ENST00000525372.5:n.1002G>A
|
|
|
ENST00000526275.5:n.1686G>A
|
|
|
ENST00000527992.5:n.1132G>A
|
|
|
ENST00000529510.5:n.592G>A
|
|
|
ENST00000530407.5:n.1054G>A
|
|
|
ENST00000532085.1:n.4285G>A
|
|
|
ENST00000538950.5:c.685G>A
|
ENSP00000475991.2:p.Gly229Ser
|
|
ENST00000545985.5:c.904G>A
|
ENSP00000475241.2:p.Gly302Ser
|
|
NM_001164277.1:c.904G>A , LRG_187t1:c.904G>A
|
NP_001157749.1:p.Gly302Ser
|
|
NM_001164278.1:c.904G>A
|
NP_001157750.1:p.Gly302Ser
|
|
NM_001164279.1:c.685G>A
|
NP_001157751.1:p.Gly229Ser
|
|
NM_001164280.1:c.904G>A
|
NP_001157752.1:p.Gly302Ser
|
|
NM_001467.5:c.904G>A
|
NP_001458.1:p.Gly302Ser
|
|
NM_001164278.2:c.904G>A
|
NP_001157750.1:p.Gly302Ser
|
|
NM_001164279.2:c.685G>A
|
NP_001157751.1:p.Gly229Ser
|
|
NM_001164280.2:c.904G>A
|
NP_001157752.1:p.Gly302Ser
|
|
NM_001467.6:c.904G>A
|
NP_001458.1:p.Gly302Ser
|
|
NM_001164277.2:c.904G>A
MANE Select
|
NP_001157749.1:p.Gly302Ser
|
|