ENST00000355773.6:c.1345C>T
MANE Select
|
ENSP00000348019.5:p.Pro449Ser
|
|
ENST00000355773.5:c.1345C>T
|
ENSP00000348019.5:p.Pro449Ser
|
|
NM_012434.4:c.1345C>T
|
NP_036566.1:p.Pro449Ser
|
|
XM_005248710.2:c.1294C>T
|
XP_005248767.1:p.Pro432Ser
|
|
XM_005248711.1:c.1147C>T
|
XP_005248768.1:p.Pro383Ser
|
|
XM_011535750.1:c.*3C>T
|
XP_011534052.1:n.*3C>T
|
|
NM_012434.5:c.1345C>T
MANE Select
|
NP_036566.1:p.Pro449Ser
|
|
NM_001382629.1:c.1114C>T
|
NP_001369558.1:p.Pro372Ser
|
|
NM_001382630.1:c.1260-5142C>T
|
NP_001369559.1:n.1260-5142C>T
|
|
NM_001382631.1:c.1366C>T
|
NP_001369560.1:p.Pro456Ser
|
|
NM_001382632.1:c.1258C>T
|
NP_001369561.1:p.Pro420Ser
|
|
NM_001382633.1:c.1345C>T
|
NP_001369562.1:p.Pro449Ser
|
|
NM_001382634.1:c.1186C>T
|
NP_001369563.1:p.Pro396Ser
|
|
NM_001382635.1:c.1342C>T
|
NP_001369564.1:p.Pro448Ser
|
|
NM_001382636.1:c.1027C>T
|
NP_001369565.1:p.Pro343Ser
|
|