ENST00000355773.6:c.1309G>T
MANE Select
|
ENSP00000348019.5:p.Gly437Ter
|
|
ENST00000355773.5:c.1309G>T
|
ENSP00000348019.5:p.Gly437Ter
|
|
NM_012434.4:c.1309G>T
|
NP_036566.1:p.Gly437Ter
|
|
XM_005248710.2:c.1258G>T
|
XP_005248767.1:p.Gly420Ter
|
|
XM_005248711.1:c.1111G>T
|
XP_005248768.1:p.Gly371Ter
|
|
XM_011535750.1:c.1161G>T
|
XP_011534052.1:p.Gln387His
|
|
NM_012434.5:c.1309G>T
MANE Select
|
NP_036566.1:p.Gly437Ter
|
|
NM_001382629.1:c.1078G>T
|
NP_001369558.1:p.Gly360Ter
|
|
NM_001382630.1:c.1260-5178G>T
|
NP_001369559.1:n.1260-5178G>T
|
|
NM_001382631.1:c.1330G>T
|
NP_001369560.1:p.Gly444Ter
|
|
NM_001382632.1:c.1222G>T
|
NP_001369561.1:p.Gly408Ter
|
|
NM_001382633.1:c.1309G>T
|
NP_001369562.1:p.Gly437Ter
|
|
NM_001382634.1:c.1150G>T
|
NP_001369563.1:p.Gly384Ter
|
|
NM_001382635.1:c.1306G>T
|
NP_001369564.1:p.Gly436Ter
|
|
NM_001382636.1:c.991G>T
|
NP_001369565.1:p.Gly331Ter
|
|