ENST00000463045.3:c.227T>G
|
ENSP00000481376.2:p.Met76Arg
|
|
ENST00000491274.6:c.356T>G
|
ENSP00000480482.2:p.Met119Arg
|
|
ENST00000375499.8:c.398T>G
MANE Select
|
ENSP00000364649.3:p.Met133Arg
|
|
ENST00000375499.7:c.398T>G
|
ENSP00000364649.3:p.Met133Arg
|
|
ENST00000463045.2:c.227T>G
|
ENSP00000481376.1:p.Met76Arg
|
|
ENST00000475506.1:n.315T>G
|
|
|
ENST00000485515.5:n.357+29T>G
|
|
|
ENST00000491274.5:c.356T>G
|
ENSP00000480482.1:p.Met119Arg
|
|
NM_003000.2:c.398T>G , LRG_316t1:c.398T>G
|
NP_002991.2:p.Met133Arg
|
|
NM_003000.3:c.398T>G
MANE Select
|
NP_002991.2:p.Met133Arg
|
|