ENST00000427724.7:c.3642A>C
|
ENSP00000390717.3:p.Ala1214=
|
|
ENST00000643257.2:c.3759A>C
MANE Select
|
ENSP00000493815.1:p.Ala1253=
|
|
ENST00000650162.1:c.3414A>C
|
ENSP00000497075.1:p.Ala1138=
|
|
ENST00000674413.1:c.3158A>C
|
|
|
ENST00000323668.11:c.3525A>C
|
ENSP00000325223.6:p.Ala1175=
|
|
ENST00000377797.7:c.3756A>C
|
ENSP00000367028.4:p.Ala1252=
|
|
ENST00000427724.6:c.3642A>C
|
ENSP00000390717.2:p.Ala1214=
|
|
ENST00000439160.6:c.3645A>C
|
ENSP00000406888.2:p.Ala1215=
|
|
ENST00000445265.6:c.3528A>C
|
ENSP00000409944.2:p.Ala1176=
|
|
ENST00000504761.6:c.3756A>C
|
ENSP00000421655.2:p.Ala1252=
|
|
ENST00000513346.5:c.3756A>C
|
ENSP00000427484.1:p.Ala1252=
|
|
ENST00000514442.5:n.3806A>C
|
|
|
ENST00000515516.1:c.343-3216A>C
|
ENSP00000426471.1:n.343-3216A>C
|
|
NM_000356.3:c.3525A>C
|
NP_000347.2:p.Ala1175=
|
|
NM_001135243.1:c.3756A>C
|
NP_001128715.1:p.Ala1252=
|
|
NM_001135244.1:c.3645A>C
|
NP_001128716.1:p.Ala1215=
|
|
NM_001135245.1:c.3528A>C
|
NP_001128717.1:p.Ala1176=
|
|
NM_001195141.1:c.3642A>C
|
NP_001182070.1:p.Ala1214=
|
|
XM_005268502.2:c.3870A>C
|
XP_005268559.1:p.Ala1290=
|
|
XM_005268503.2:c.3867A>C
|
XP_005268560.1:p.Ala1289=
|
|
XM_005268504.2:c.3867A>C
|
XP_005268561.1:p.Ala1289=
|
|
XM_005268505.2:c.3759A>C
|
XP_005268562.1:p.Ala1253=
|
|
XM_005268506.2:c.3756A>C
|
XP_005268563.1:p.Ala1252=
|
|
XM_005268507.2:c.3639A>C
|
XP_005268564.1:p.Ala1213=
|
|
XM_011537678.1:c.3690A>C
|
XP_011535980.1:p.Ala1230=
|
|
XM_005268502.4:c.3870A>C
|
XP_005268559.1:p.Ala1290=
|
|
XM_005268503.4:c.3867A>C
|
XP_005268560.1:p.Ala1289=
|
|
XM_005268504.4:c.3867A>C
|
XP_005268561.1:p.Ala1289=
|
|
XM_005268505.4:c.3759A>C
|
XP_005268562.1:p.Ala1253=
|
|
XM_005268506.4:c.3756A>C
|
XP_005268563.1:p.Ala1252=
|
|
XM_005268507.4:c.3639A>C
|
XP_005268564.1:p.Ala1213=
|
|
XM_011537678.3:c.3690A>C
|
XP_011535980.1:p.Ala1230=
|
|
XM_017009792.2:c.3753A>C
|
XP_016865281.1:p.Ala1251=
|
|
XM_017009793.2:c.3579A>C
|
XP_016865282.1:p.Ala1193=
|
|
XM_017009794.2:c.3465A>C
|
XP_016865283.1:p.Ala1155=
|
|
XR_427778.3:n.3876A>C
|
|
|
XR_427780.3:n.3765A>C
|
|
|
NM_000356.4:c.3525A>C
|
NP_000347.2:p.Ala1175=
|
|
NM_001135244.2:c.3645A>C
|
NP_001128716.1:p.Ala1215=
|
|
NM_001135245.2:c.3528A>C
|
NP_001128717.1:p.Ala1176=
|
|
NM_001195141.2:c.3642A>C
|
NP_001182070.1:p.Ala1214=
|
|
NM_001371623.1:c.3759A>C
MANE Select
|
NP_001358552.1:p.Ala1253=
|
|
NM_001135243.2:c.3756A>C
|
NP_001128715.1:p.Ala1252=
|
|