ENST00000675795.1:c.1040C>G
MANE Select
|
ENSP00000501699.1:p.Pro347Arg
|
|
ENST00000286301.7:c.1040C>G
|
ENSP00000286301.3:p.Pro347Arg
|
|
ENST00000504875.5:c.1040C>G
|
ENSP00000422212.1:p.Pro347Arg
|
|
ENST00000543093.1:c.890-2772C>G
|
ENSP00000445282.1:n.890-2772C>G
|
|
NM_001288705.1:c.1040C>G
|
NP_001275634.1:p.Pro347Arg
|
|
NM_005211.3:c.1040C>G
|
NP_005202.2:p.Pro347Arg
|
|
NR_109969.1:n.1253C>G
|
|
|
NM_001288705.2:c.1040C>G
|
NP_001275634.1:p.Pro347Arg
|
|
NM_001349736.1:c.1040C>G
|
NP_001336665.1:p.Pro347Arg
|
|
NM_001288705.3:c.1040C>G
MANE Select
|
NP_001275634.1:p.Pro347Arg
|
|
NM_001375320.1:c.1040C>G
|
NP_001362249.1:p.Pro347Arg
|
|
NM_001375321.1:c.596C>G
|
NP_001362250.1:p.Pro199Arg
|
|
NR_164679.1:n.1096C>G
|
|
|
NM_001349736.2:c.1040C>G
|
NP_001336665.1:p.Pro347Arg
|
|
NM_005211.4:c.1040C>G
|
NP_005202.2:p.Pro347Arg
|
|
NR_109969.2:n.1167C>G
|
|
|