ENST00000355773.6:c.1346C>A
MANE Select
|
ENSP00000348019.5:p.Pro449His
|
|
ENST00000355773.5:c.1346C>A
|
ENSP00000348019.5:p.Pro449His
|
|
NM_012434.4:c.1346C>A
|
NP_036566.1:p.Pro449His
|
|
XM_005248710.2:c.1295C>A
|
XP_005248767.1:p.Pro432His
|
|
XM_005248711.1:c.1148C>A
|
XP_005248768.1:p.Pro383His
|
|
XM_011535750.1:c.*4C>A
|
XP_011534052.1:n.*4C>A
|
|
NM_012434.5:c.1346C>A
MANE Select
|
NP_036566.1:p.Pro449His
|
|
NM_001382629.1:c.1115C>A
|
NP_001369558.1:p.Pro372His
|
|
NM_001382630.1:c.1260-5141C>A
|
NP_001369559.1:n.1260-5141C>A
|
|
NM_001382631.1:c.1367C>A
|
NP_001369560.1:p.Pro456His
|
|
NM_001382632.1:c.1259C>A
|
NP_001369561.1:p.Pro420His
|
|
NM_001382633.1:c.1346C>A
|
NP_001369562.1:p.Pro449His
|
|
NM_001382634.1:c.1187C>A
|
NP_001369563.1:p.Pro396His
|
|
NM_001382635.1:c.1343C>A
|
NP_001369564.1:p.Pro448His
|
|
NM_001382636.1:c.1028C>A
|
NP_001369565.1:p.Pro343His
|
|