ENST00000355773.6:c.1307C>G
MANE Select
|
ENSP00000348019.5:p.Pro436Arg
|
|
ENST00000355773.5:c.1307C>G
|
ENSP00000348019.5:p.Pro436Arg
|
|
NM_012434.4:c.1307C>G
|
NP_036566.1:p.Pro436Arg
|
|
XM_005248710.2:c.1256C>G
|
XP_005248767.1:p.Pro419Arg
|
|
XM_005248711.1:c.1109C>G
|
XP_005248768.1:p.Pro370Arg
|
|
XM_011535750.1:c.1159C>G
|
XP_011534052.1:p.Gln387Glu
|
|
NM_012434.5:c.1307C>G
MANE Select
|
NP_036566.1:p.Pro436Arg
|
|
NM_001382629.1:c.1076C>G
|
NP_001369558.1:p.Pro359Arg
|
|
NM_001382630.1:c.1260-5180C>G
|
NP_001369559.1:n.1260-5180C>G
|
|
NM_001382631.1:c.1328C>G
|
NP_001369560.1:p.Pro443Arg
|
|
NM_001382632.1:c.1220C>G
|
NP_001369561.1:p.Pro407Arg
|
|
NM_001382633.1:c.1307C>G
|
NP_001369562.1:p.Pro436Arg
|
|
NM_001382634.1:c.1148C>G
|
NP_001369563.1:p.Pro383Arg
|
|
NM_001382635.1:c.1304C>G
|
NP_001369564.1:p.Pro435Arg
|
|
NM_001382636.1:c.989C>G
|
NP_001369565.1:p.Pro330Arg
|
|