ENST00000476864.2:c.1218T>C
|
ENSP00000452319.2:p.Asn406=
|
|
ENST00000700414.1:c.*1069T>C
|
ENSP00000514978.1:n.*1069T>C
|
|
ENST00000700415.1:c.1128T>C
|
ENSP00000514979.1:p.Asn376=
|
|
ENST00000700417.1:c.1146T>C
|
ENSP00000514981.1:p.Asn382=
|
|
ENST00000700444.1:c.*987T>C
|
ENSP00000514992.1:n.*987T>C
|
|
ENST00000303635.12:c.1218T>C
MANE Select
|
ENSP00000306522.6:p.Asn406=
|
|
ENST00000303635.11:c.1218T>C
|
ENSP00000306522.6:p.Asn406=
|
|
NM_015215.3:c.1218T>C
|
NP_056030.1:p.Asn406=
|
|
XM_011541083.1:c.1218T>C
|
XP_011539385.1:p.Asn406=
|
|
XM_011541084.1:c.1218T>C
|
XP_011539386.1:p.Asn406=
|
|
XM_011541085.1:c.1206T>C
|
XP_011539387.1:p.Asn402=
|
|
XM_011541086.1:c.1218T>C
|
XP_011539388.1:p.Asn406=
|
|
XM_011541087.1:c.1146T>C
|
XP_011539389.1:p.Asn382=
|
|
XM_011541088.1:c.1128T>C
|
XP_011539390.1:p.Asn376=
|
|
XM_011541089.1:c.1218T>C
|
XP_011539391.1:p.Asn406=
|
|
XM_011541090.1:c.1218T>C
|
XP_011539392.1:p.Asn406=
|
|
XM_011541091.1:c.1218T>C
|
XP_011539393.1:p.Asn406=
|
|
XM_011541092.1:c.1218T>C
|
XP_011539394.1:p.Asn406=
|
|
NM_001349608.1:c.1128T>C
|
NP_001336537.1:p.Asn376=
|
|
NM_001349609.1:c.1218T>C
|
NP_001336538.1:p.Asn406=
|
|
NM_001349610.1:c.1218T>C
|
NP_001336539.1:p.Asn406=
|
|
NM_001349612.1:c.1128T>C
|
NP_001336541.1:p.Asn376=
|
|
XM_011541083.2:c.1218T>C
|
XP_011539385.1:p.Asn406=
|
|
XM_011541084.2:c.1218T>C
|
XP_011539386.1:p.Asn406=
|
|
XM_011541086.3:c.1218T>C
|
XP_011539388.1:p.Asn406=
|
|
XM_011541087.2:c.1146T>C
|
XP_011539389.1:p.Asn382=
|
|
XM_011541088.2:c.1128T>C
|
XP_011539390.1:p.Asn376=
|
|
XM_011541090.3:c.1218T>C
|
XP_011539392.1:p.Asn406=
|
|
XM_011541091.2:c.1218T>C
|
XP_011539393.1:p.Asn406=
|
|
XM_011541092.3:c.1218T>C
|
XP_011539394.1:p.Asn406=
|
|
XM_017000774.2:c.1218T>C
|
XP_016856263.1:p.Asn406=
|
|
XM_017000777.1:c.1218T>C
|
XP_016856266.1:p.Asn406=
|
|
XM_017000778.1:c.1218T>C
|
XP_016856267.1:p.Asn406=
|
|
NM_015215.4:c.1218T>C
MANE Select
|
NP_056030.1:p.Asn406=
|
|
NM_001349608.2:c.1128T>C
|
NP_001336537.1:p.Asn376=
|
|
NM_001349609.2:c.1218T>C
|
NP_001336538.1:p.Asn406=
|
|
NM_001349610.2:c.1218T>C
|
NP_001336539.1:p.Asn406=
|
|
NM_001349612.2:c.1128T>C
|
NP_001336541.1:p.Asn376=
|
|