ENST00000623535.2:c.2846T>G
MANE Select
|
ENSP00000485244.1:p.Met949Arg
|
|
ENST00000674046.1:c.2969T>G
|
ENSP00000501174.1:p.Met990Arg
|
|
ENST00000379989.6:c.2713+133T>G
|
ENSP00000369325.3:n.2713+133T>G
|
|
ENST00000379996.7:c.2713+133T>G
|
ENSP00000369332.3:n.2713+133T>G
|
|
ENST00000623535.1:c.2846T>G
|
ENSP00000485244.1:p.Met949Arg
|
|
NM_001037343.1:c.2713+133T>G
|
NP_001032420.1:n.2713+133T>G
|
|
NM_003159.2:c.2713+133T>G
|
NP_003150.1:n.2713+133T>G
|
|
XM_011545569.1:c.2785+133T>G
|
XP_011543871.1:n.2785+133T>G
|
|
XM_011545570.1:c.2704+133T>G
|
XP_011543872.1:n.2704+133T>G
|
|
XR_950484.1:n.3088+133T>G
|
|
|
NM_001323289.1:c.2846T>G
|
NP_001310218.1:p.Met949Arg
|
|
NM_001323289.2:c.2846T>G
MANE Select
|
NP_001310218.1:p.Met949Arg
|
|
NM_001037343.2:c.2713+133T>G
|
NP_001032420.1:n.2713+133T>G
|
|
NM_003159.3:c.2713+133T>G
|
NP_003150.1:n.2713+133T>G
|
|