ENST00000355773.6:c.1322C>A
MANE Select
|
ENSP00000348019.5:p.Pro441His
|
|
ENST00000355773.5:c.1322C>A
|
ENSP00000348019.5:p.Pro441His
|
|
NM_012434.4:c.1322C>A
|
NP_036566.1:p.Pro441His
|
|
XM_005248710.2:c.1271C>A
|
XP_005248767.1:p.Pro424His
|
|
XM_005248711.1:c.1124C>A
|
XP_005248768.1:p.Pro375His
|
|
XM_011535750.1:c.1174C>A
|
XP_011534052.1:p.Pro392Thr
|
|
NM_012434.5:c.1322C>A
MANE Select
|
NP_036566.1:p.Pro441His
|
|
NM_001382629.1:c.1091C>A
|
NP_001369558.1:p.Pro364His
|
|
NM_001382630.1:c.1260-5165C>A
|
NP_001369559.1:n.1260-5165C>A
|
|
NM_001382631.1:c.1343C>A
|
NP_001369560.1:p.Pro448His
|
|
NM_001382632.1:c.1235C>A
|
NP_001369561.1:p.Pro412His
|
|
NM_001382633.1:c.1322C>A
|
NP_001369562.1:p.Pro441His
|
|
NM_001382634.1:c.1163C>A
|
NP_001369563.1:p.Pro388His
|
|
NM_001382635.1:c.1319C>A
|
NP_001369564.1:p.Pro440His
|
|
NM_001382636.1:c.1004C>A
|
NP_001369565.1:p.Pro335His
|
|