ENST00000355773.6:c.1301C>G
MANE Select
|
ENSP00000348019.5:p.Thr434Ser
|
|
ENST00000355773.5:c.1301C>G
|
ENSP00000348019.5:p.Thr434Ser
|
|
NM_012434.4:c.1301C>G
|
NP_036566.1:p.Thr434Ser
|
|
XM_005248710.2:c.1250C>G
|
XP_005248767.1:p.Thr417Ser
|
|
XM_005248711.1:c.1103C>G
|
XP_005248768.1:p.Thr368Ser
|
|
XM_011535750.1:c.1153C>G
|
XP_011534052.1:p.Leu385Val
|
|
NM_012434.5:c.1301C>G
MANE Select
|
NP_036566.1:p.Thr434Ser
|
|
NM_001382629.1:c.1070C>G
|
NP_001369558.1:p.Thr357Ser
|
|
NM_001382630.1:c.1260-5186C>G
|
NP_001369559.1:n.1260-5186C>G
|
|
NM_001382631.1:c.1322C>G
|
NP_001369560.1:p.Thr441Ser
|
|
NM_001382632.1:c.1214C>G
|
NP_001369561.1:p.Thr405Ser
|
|
NM_001382633.1:c.1301C>G
|
NP_001369562.1:p.Thr434Ser
|
|
NM_001382634.1:c.1142C>G
|
NP_001369563.1:p.Thr381Ser
|
|
NM_001382635.1:c.1298C>G
|
NP_001369564.1:p.Thr433Ser
|
|
NM_001382636.1:c.983C>G
|
NP_001369565.1:p.Thr328Ser
|
|