ENST00000355773.6:c.1322C>G
MANE Select
|
ENSP00000348019.5:p.Pro441Arg
|
|
ENST00000355773.5:c.1322C>G
|
ENSP00000348019.5:p.Pro441Arg
|
|
NM_012434.4:c.1322C>G
|
NP_036566.1:p.Pro441Arg
|
|
XM_005248710.2:c.1271C>G
|
XP_005248767.1:p.Pro424Arg
|
|
XM_005248711.1:c.1124C>G
|
XP_005248768.1:p.Pro375Arg
|
|
XM_011535750.1:c.1174C>G
|
XP_011534052.1:p.Pro392Ala
|
|
NM_012434.5:c.1322C>G
MANE Select
|
NP_036566.1:p.Pro441Arg
|
|
NM_001382629.1:c.1091C>G
|
NP_001369558.1:p.Pro364Arg
|
|
NM_001382630.1:c.1260-5165C>G
|
NP_001369559.1:n.1260-5165C>G
|
|
NM_001382631.1:c.1343C>G
|
NP_001369560.1:p.Pro448Arg
|
|
NM_001382632.1:c.1235C>G
|
NP_001369561.1:p.Pro412Arg
|
|
NM_001382633.1:c.1322C>G
|
NP_001369562.1:p.Pro441Arg
|
|
NM_001382634.1:c.1163C>G
|
NP_001369563.1:p.Pro388Arg
|
|
NM_001382635.1:c.1319C>G
|
NP_001369564.1:p.Pro440Arg
|
|
NM_001382636.1:c.1004C>G
|
NP_001369565.1:p.Pro335Arg
|
|